Primary Ciliary DyskinesiaNCT06959251
Glycine and Magnesium+Thiamine for the Treatment of Primary Ciliary Dyskinesia
A study testing Glycine and Magnesium+thiamine in people with Primary Ciliary Dyskinesia, run by Instituto Nacional de Enfermedades Respiratorias at 1 site in Mexico.
Trial summary
Patients with primary ciliary dyskinesia (PCD) have trouble with clearing their bronchi from mucus, which in the long-term may produce severe damage to the lungs. Currently, there is no specific treatment for PCD beyond supportive measures such as airway hydration and postural drainage. Read more about this study
- Who is it for?
- Ages 5 years and older
- Conditions the study is for
- Primary Ciliary Dyskinesia
- What is being tested?
- Glycine and Magnesium+thiamine
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 60 participants
- Where
- 1 siteMexico
- Study dates
- 2 Oct 2025to Mar 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 5 years and older
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Any sex.
- Age of 5 years or more.
- Diagnosis of primary ciliary dyskinesia (PCD) established according to international recommendations (Shapiro et al. Am J Respir Crit Care Med 2018;197(12):e24-e39, and Shapiro et al. Ped Pulmonol 2016;51:115-132).
- Without respiratory exacerbations of PCD in the previous 30 days.
- Without acute respiratory infection in the previous 30 days.
- Informed consent letter signed by the patient (if the patient's age is 18 years or more).
- Informed consent letter signed by the legal guardian, and assent letter signed by the patient (if the patient's age is <18 years).
Who cannot join
- 1. Participation in other research protocol involving therapeutic measures.
- Elimination Criteria:
- 1. None.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Mexico1 site, 1 recruiting
- Recruiting
Instituto Nacional de Enfermedades Respiratorias
Mexico City, 14080
Mario H. Vargas, MSc, 5556665868, mhvargasb@yahoo.com.mx
Mario H. Vargas, MD, MSc
About this study
Official title: A Randomized, Placebo-controlled Clinical Trial Evaluating the Efficacy and Safety of Glycine and Magnesium+Thiamine Supplements, Alone or Combined, Administered for 6 Months to Patients With Primary Ciliary Dyskinesia
- Patients with primary ciliary dyskinesia (PCD) have trouble with clearing their bronchi from mucus, which in the long-term may produce severe damage to the lungs. Currently, there is no specific treatment for PCD beyond supportive measures such as airway hydration and postural drainage.
- Glycine is an amino acid with anti-inflammatory properties that proved to be beneficial in another disease with problematic airway clearance, cystic fibrosis.
- Magnesium participates in many crucial chemical reactions, including some that might favor fluidification and mobilization of mucus. Thiamine (vitamin B1) co-participates with magnesium in some mitochondrial enzymatic reactions occurring in the citric acid cycle.
- Thus, oral supplements of glycine and magnesium+thiamine might improve symptoms and lung function of patients with PCD, and these effects may even be better if these supplements are combined.
- In this study, in addition to their usual care, patients with PCD will receive for 6 months one of the following treatments: 1) an oral supplement of 0.5 g/kg/day glycine, 2) an oral supplement of up to 400 mg/day elementary magnesium plus up to 10 mg/day thiamine, according to the subject's age, 3) glycine plus magnesium+thiamine supplements, as described, or 4) a placebo, which is an inert substance. All treatments will be administered as a whitish powder contained in similar bottles.
- The investigators will evaluate whether glycine and/or magnesium+thiamine reduce exacerbations of the disease, improve pulmonary function and quality of life, and reduce some pro-inflammatory compounds measured in saliva.
Read the detailed description
Background Primary ciliary dyskinesia (PCD) is characterized by ciliary dysfunction causing mucus accumulation in the airways that favors recurrent infections and bronchiectasis. Apart from general airway clearance, few therapeutic alternatives exist for PCD, and these are usually derived from experiences obtained from other lung diseases such as cystic fibrosis. Among the few clinical trials focused on PCD, the use of azithromycin for 6 months decreased the number of respiratory exacerbations, but with little or no impact on lung function or quality of life. Likewise, although useful in cystic fibrosis, inhalation of hypertonic saline and oral administration of N-acetylcysteine did not improve respiratory symptoms in patients with PCD. Therefore, it is urgent to find therapeutic approaches that prevent respiratory exacerbations, improve quality of life and, ideally, improve lung function. A lot of scientific literature supports the potential beneficial effect of glycine and/or magnesium+thiamine supplements in patients with PCD, as described below. Thus, in this study the investigators will evaluate the effect of glycine and magnesium+thiamine supplementation, alone or combined, in patients with PCD.
Characteristics of glycine Glycine is a non-essential and the simplest amino acid. Physically, it is a whitish powder with a sweet taste, soluble in water and relatively inexpensive (approximately $27 dollars per kg). Aside from participating in protein composition, glycine is an agonist for its own specific receptors (GlyR), which are chloride channels that cause membrane hyperpolarization. In excitable cells such as neurons, glycine is an inhibitory neurotransmitter, while in other cells such as Kupffer cells, alveolar macrophages and neutrophils, this amino acid reduces the sensitivity to proinflammatory stimuli. This stabilizing effect on inflammatory cells has been corroborated in several studies. For example, glycine decreases the expression and levels of tumor necrosis factor (TNF)-α and IL-6 in mouse adipose tissue and prevents the production of TNF-α and superoxide anion in lipopolysaccharide-stimulated alveolar macrophages, as well as TNF-α and IL-6 in 3T3-L1 cells, probably through the inhibition of IKK-α/β and, therefore, of NF-kB phosphorylation. In animal models of endotoxic shock, glycine protects from structural damage and decreases neutrophilic inflammation and proinflammatory cytokine production, probably through inhibition of NF-kB and NLRP3, as well as restoration of NRF2. Recently, in a controlled, crossover clinical trial the investigators administered 0.5 g/kg/day of glycine orally for 8 weeks to children with cystic fibrosis (Vargas et al. BMC Pulm Med 2017;17(1):206. doi: 10.1186/s12890-017-0528-x). This study demonstrated that glycine induced an improvement in clinical and spirometric variables, as well as a decrease in serum TNF-α and a trend towards a decrease in IL-6 and G-CSF. In this and many other studies, oral glycine was virtually devoid of adverse effects.
Possible role of magnesium and thiamine in PCD Epidemiological studies have shown that hypomagnesemia is highly prevalent in the general population, even among self-reported healthy individuals, being as high as 30%. This can be explained by several factors, including Western-type diet, decreased concentration of magnesium in vegetables, use of medications that decrease the intestinal absorption of magnesium or favor its renal elimination, and genetic variants of magnesium transport proteins. Therefore, in patients with PCD, it is expected that at least a similar percentage have a magnesium deficiency. In humans, magnesium is an indispensable element for the proper functioning of at least 300 enzymes involved in vital processes, including those involved in relevant intracellular signaling pathways, for example, kinases (which phosphorylate substrates from ATP-Mg2+), adenylate cyclase (which generates the second messenger cyclic AMP) and G proteins (key GTPases in intracellular signaling of many receptors). Therefore, a relative magnesium deficiency could affect the function of virtually any tissue. In addition, it has been shown that the activity of exogenous rhDNase or endogenous DNases require magnesium in the microenvironment. On the other hand, magnesium is an indispensable cofactor for ATP (ATP-Mg2+) to be utilized by the ATPase domain of dynein and to generate the ciliary beating movement. Therefore, magnesium is important also for mucous fluidification and ciliary functioning. Finally, one of the most relevant metabolic pathways where magnesium is essential is the citric acid cycle, which is the main energy (ATP) generator in the mitochondria, since it is a cofactor of pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase and branched-chain keto amino acid dehydrogenase, as well as other related enzymes such as transketolase and 2-hydroxyacyl CoA lyase. It is important to note that in addition to magnesium, all these enzymes also require thiamine diphosphate, so that the deficiency of either cofactor (magnesium and thiamine) leads to mitochondrial dysfunction. This is particularly relevant in PCD because proper mitochondrial function is essential for the formation and functioning of cilia.
Hypothesis
- In patients with PCD, glycine or magnesium+thiamine supplementation for 6 months will be associated with a 25% decrease in the number of respiratory exacerbations compared to placebo.
- In patients with PCD, combined glycine and magnesium+thiamine supplements for 6 months will be associated with a 50% decrease in the number of respiratory exacerbations compared to placebo.
Major objective To evaluate the effect of glycine and magnesium+thiamine supplements, alone or combined, administered for 6 months to patients with PCD on the number of respiratory exacerbations.
Secondary objectives
To evaluate the effect of glycine and magnesium+thiamine supplements, alone or combined, administered for 6 months to patients with PCD on:
- Quality of life (questionnaire of the Spanish version of the QOL-PCD, as well as some questions on possible side effects).
- Growth and development (weight-for-height, height-for-age, BMI).
- Peripheral oxygen saturation (SpO2).
- Pulmonary function tests (nasal nitric oxide, oscillometry, multiple breath nitrogen washout, spirometry, 6-min walking test).
- Biomarkers in saliva (IL-1β, IL-6, IL-8, TNF-α, MPO).
Description of the study The study will be carried out at the Instituto Nacional de Enfermedades Respiratorias (INER), located in Mexico City. Once an informed consent is signed by patients or their legal guardians, participants will be randomly allocated to one of four study arms: 1) glycine, 2) magnesium+thiamine, 3) glycine and magnesium+thiamine, 4) placebo. Glycine will be administered at a dose of 0.5 g/kg/day, up to a maximum of 25 g/day. The dose of magnesium will be 8 mg/kg/day of elementary magnesium administered as magnesium citrate, up to a maximum of 400 mg/day. The dose of thiamine will be 0.2 mg/kg/day administered as benfotiamine, up to a maximum of 10 mg/day. Patients or their legal guardians will be asked to fill out an online symptom questionnaire every week. At the initial visit and every 2 months the following maneuvers will be performed: inquiry about pulmonary exacerbations; weight and height measurements; physical examination; pulse oximetry; saliva sampling for measuring IL-1β, IL-6, IL-8, TNF-α, myeloperoxidase (MPO) and albumin; nasal nitric oxide measurement; basal oscillometry; multiple breath nitrogen washout test; basal spirometry; post-salbutamol oscillometry and spirometry, 6-min walk test. In each visit, except for the final visit, a 500 g plastic bottle with a mixture of glycine, magnesium+thiamine, and/or placebo (sugar glass) powders, according to their assigned group, will be given to the patient or to the person at charge. All bottles will be identical in appearance.
Sample size Due to feasibility reasons, the investigators consider that the number of participants in each of the four groups will be n=15 (total n=60 patients).
- Conditions
- Primary Ciliary Dyskinesia
- Being tested
- Glycine, Magnesium+thiamine, Placebo
- Keywords
- Primary ciliary dyskinesia, Glycine, Magnesium, Lung function, thiamine, benfotiamine
- Medical subject headings
- Ciliary Motility Disorders
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
GlycineDietary supplement
Patients will receive for 6 months an oral supplement of 0.5 g/kg/day glycine, up to 25 g/day, divided in three daily intakes.
Magnesium+thiamineDietary supplement
Patients will receive for 6 months an oral supplement of up to 400 mg/day, according to age, of elementary magnesium (formulated as magnesium citrate) plus up to 10 mg/day of thiamine (formulated as benfotiamine), divided in three daily intakes.
PlaceboOther
Patients will receive for 6 months placebo (sugar glass), in a similar daily amount as in experimental arms, and divided in three daily intakes.
| Study group | Role | What they receive |
|---|---|---|
| Glycine | Experimental | Patients will receive for 6 months an oral supplement of 0.5 g/kg/day glycine, up to 25 g/day, divided in three daily intakes. Receives: Dietary Supplement: Glycine |
| Magnesium+thiamine | Experimental | Patients will receive for 6 months an oral supplement of up to 400 mg/day, according to age, of elementary magnesium (formulated as magnesium citrate) plus up to 10 mg/day of thiamine (formulated as benfotiamine), divided in three daily intakes. Receives: Dietary Supplement: Magnesium+thiamine |
| Glycine plus magnesium+thiamine | Experimental | Patients will receive for 6 months oral supplements of glycine and magnesium+thiamine, as described. Receives: Dietary Supplement: Glycine; Dietary Supplement: Magnesium+thiamine |
| Placebo | Placebo comparator | Patients will receive for 6 months placebo (sugar glass), in a similar daily amount as in experimental arms, and divided in three daily intakes. Receives: Other: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of respiratory exacerbations
A respiratory exacerbation will be defined as: 1) any increase in respiratory symptoms that motivated the initiation of antibiotic therapy, or 2) a 10% or more decrease in FEV1 with respect to the FEV1 value at recruitment. A blinded pediatric pulmonologist will review all cases to corroborate whether a suspected episode was indeed a respiratory exacerbation.
Measured: 6 months
Secondary outcomes (26)
Quality of life-Primary ciliary dyskinesia questionnaire (QOL-PCD)
The quality of life will be assessed weekly by the Spanish version of the QOL-PCD questionnaire, as well as by some questions on possible side effects, filled online.
Measured: 6 months
Weight-for-height
The z score of weight-for-height will be used as a proxy for assessing the child's growth and development every two months.
Measured: 6 months
Height-for-age
The z score of height-for-age will be used as a proxy for assessing the child's growth and development every two months.
Measured: 6 months
SpO2
Peripheral blood oxygen saturation, as measured by pulse oximetry every two months.
Measured: 6 months
Body mass index
The z score of body mass index will be used as a proxy for assessing the child's growth and development every two months
Measured: 6 months
Nasal nitric oxide
The level (nL/min) of nasal nitric oxide measured every two months.
Measured: 6 months
R5
Respiratory system resistance in kPa/(L/s) measured every two months by impulse oscillometry at 5 Hz (a proxy of total airway resistance).
Measured: 6 months
R20
Respiratory system resistance in kPa/(L/s) measured every two months by impulse oscillometry at 20 Hz (a proxy of large airway resistance).
Measured: 6 months
R5-R20
Difference between respiratory system resistances at 5 and 20 Hz, measured every two months by impulse oscillometry (a proxy of peripheral airway resistance).
Measured: 6 months
(R5-R20)/R5
Difference between respiratory system resistances at 5 and 20 Hz, divided by R5, measured every two months by impulse oscillometry (a proxy of peripheral airway resistance).
Measured: 6 months
X5
Respiratory system reactance in kPa/(L/s) measured every two months by impulse oscillometry at 5 Hz (a proxy of lung parenchyma/peripheral airway status).
Measured: 6 months
X20
Respiratory system reactance in kPa/(L/s) measured every two months by impulse oscillometry at 20 Hz (a proxy of lung parenchyma/peripheral airway status).
Measured: 6 months
Frequency of resonance (Fres)
Hz at which lung elastance and inertance are in equilibrium, as measured every two months by impulse oscillometry.
Measured: 6 months
Area of reactance (AX)
Area, in kPa/L, limited below by X5 and Fres, and above by the zero reactance, as measured every two months by impulse oscillometry.
Measured: 6 months
Multiple breath nitrogen washout
Lung clearance index measured every two months by multiple breath nitrogen washout.
Measured: 6 months
FVC
Forced vital capacity, measured every two months by spirometry.
Measured: 6 months
FEV1
Forced expiratory volume at the first second, measured every two months by spirometry.
Measured: 6 months
FEV1/FVC
Ratio of forced expiratory volume at the first second and forced vital capacity, measured every two months by spirometry.
Measured: 6 months
Response to bronchodilator (oscillometry)
Change in lung function, as assessed by oscillometry, after the inhalation of a bronchodilator (salbutamol), measured every two months.
Measured: 6 months
Response to bronchodilator (spirometry)
Change in lung function, as assessed by spirometry, after the inhalation of a bronchodilator (salbutamol), measured every two months.
Measured: 6 months
6-minute walk test
Exercise test performed every two months in which the subject walks in a flat surface for 6 minutes to evaluate the maximum distance achieved.
Measured: 6 months
IL-1beta in saliva
Interleukin 1 beta, measured in a saliva sample.
Measured: 6 months
IL-6 in saliva
Interleukin 6, measured in a saliva sample.
Measured: 6 months
IL-8 in saliva
Interleukin 8, measured in a saliva sample.
Measured: 6 months
TNF-alpha in saliva
Tumor necrosis factor alpha, measured in a saliva sample.
Measured: 6 months
MPO in saliva
Neutrophilic myeloperoxidase, measured in a saliva sample.
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 May 2025
- Study start2 Oct 2025
- Primary completionMar 2028 (estimated)
- Study completionMar 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (43)Papers the sponsor has linked to this study.
- Other trials for Primary Ciliary DyskinesiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Four arms, parallel design, placebo controlled.
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 60 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Instituto Nacional de Enfermedades Respiratorias
- Sponsor type
- Other government
- Responsible party
- Principal investigator, Mario H. Vargas, Instituto Nacional de Enfermedades Respiratorias
- Investigators
- Mario H. Vargas, MSc, Principal investigator, 5556665868
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06959251
- Sponsor's protocol ID
- C16-24
- Status last verified
- Oct 2025
- First submitted
- 28 Apr 2025
- Last updated
- 25 Nov 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: Data will be available upon reasonable request for research purposes.
Publications
Piatti G, De Santi MM, Farolfi A, Zuccotti GV, D'Auria E, Patria MF, Torretta S, Consonni D, Ambrosetti U. Exacerbations and Pseudomonas aeruginosa colonization are associated with altered lung structure and function in primary ciliary dyskinesia. BMC Pediatr. 2020 Apr 13;20(1):158. doi: 10.1186/s12887-020-02062-4.
PubMed 32284045Sagel SD, Kupfer O, Wagner BD, Davis SD, Dell SD, Ferkol TW, Hoppe JE, Rosenfeld M, Sullivan KM, Tiddens HAWM, Knowles MR, Leigh MW. Airway Inflammation in Children with Primary Ciliary Dyskinesia. Ann Am Thorac Soc. 2023 Jan;20(1):67-74. doi: 10.1513/AnnalsATS.202204-314OC.
PubMed 35984413Gontijo-Amaral C, Guimaraes EV, Camargos P. Oral magnesium supplementation in children with cystic fibrosis improves clinical and functional variables: a double-blind, randomized, placebo-controlled crossover trial. Am J Clin Nutr. 2012 Jul;96(1):50-6. doi: 10.3945/ajcn.112.034207. Epub 2012 May 30.
PubMed 22648717Vargas MH, Del-Razo-Rodriguez R, Lopez-Garcia A, Lezana-Fernandez JL, Chavez J, Furuya MEY, Marin-Santana JC. Effect of oral glycine on the clinical, spirometric and inflammatory status in subjects with cystic fibrosis: a pilot randomized trial. BMC Pulm Med. 2017 Dec 15;17(1):206. doi: 10.1186/s12890-017-0528-x.
PubMed 29246256Kobbernagel HE, Buchvald FF, Haarman EG, Casaulta C, Collins SA, Hogg C, Kuehni CE, Lucas JS, Moser CE, Quittner AL, Raidt J, Rosthoj S, Sorensen AL, Thomsen K, Werner C, Omran H, Nielsen KG. Efficacy and safety of azithromycin maintenance therapy in primary ciliary dyskinesia (BESTCILIA): a multicentre, double-blind, randomised, placebo-controlled phase 3 trial. Lancet Respir Med. 2020 May;8(5):493-505. doi: 10.1016/S2213-2600(20)30058-8.
PubMed 32380069Paff T, Daniels JM, Weersink EJ, Lutter R, Vonk Noordegraaf A, Haarman EG. A randomised controlled trial on the effect of inhaled hypertonic saline on quality of life in primary ciliary dyskinesia. Eur Respir J. 2017 Feb 23;49(2):1601770. doi: 10.1183/13993003.01770-2016. Print 2017 Feb.
PubMed 28232410Jensen T, Kharazmi A, Schiotz PO, Nielsen H, Stenvang Pedersen S, Stafanger G, Koch C, Hoiby N. Effect of oral N-acetylcysteine administration on human blood neutrophil and monocyte function. APMIS. 1988 Jan;96(1):62-7. doi: 10.1111/j.1699-0463.1988.tb05269.x.
PubMed 3345250Jentsch TJ, Stein V, Weinreich F, Zdebik AA. Molecular structure and physiological function of chloride channels. Physiol Rev. 2002 Apr;82(2):503-68. doi: 10.1152/physrev.00029.2001.
PubMed 11917096Van den Eynden J, Ali SS, Horwood N, Carmans S, Brone B, Hellings N, Steels P, Harvey RJ, Rigo JM. Glycine and glycine receptor signalling in non-neuronal cells. Front Mol Neurosci. 2009 Aug 20;2:9. doi: 10.3389/neuro.02.009.2009. eCollection 2009.
PubMed 19738917Wheeler MD, Rose ML, Yamashima S, Enomoto N, Seabra V, Madren J, Thurman RG. Dietary glycine blunts lung inflammatory cell influx following acute endotoxin. Am J Physiol Lung Cell Mol Physiol. 2000 Aug;279(2):L390-8. doi: 10.1152/ajplung.2000.279.2.L390.
PubMed 10926563Alarcon-Aguilar FJ, Almanza-Perez J, Blancas G, Angeles S, Garcia-Macedo R, Roman R, Cruz M. Glycine regulates the production of pro-inflammatory cytokines in lean and monosodium glutamate-obese mice. Eur J Pharmacol. 2008 Dec 3;599(1-3):152-8. doi: 10.1016/j.ejphar.2008.09.047. Epub 2008 Oct 9.
PubMed 18930730Almanza-Perez JC, Alarcon-Aguilar FJ, Blancas-Flores G, Campos-Sepulveda AE, Roman-Ramos R, Garcia-Macedo R, Cruz M. Glycine regulates inflammatory markers modifying the energetic balance through PPAR and UCP-2. Biomed Pharmacother. 2010 Oct;64(8):534-40. doi: 10.1016/j.biopha.2009.04.047. Epub 2009 Oct 17.
PubMed 19864106Wheeler MD, Thurman RG. Production of superoxide and TNF-alpha from alveolar macrophages is blunted by glycine. Am J Physiol. 1999 Nov;277(5):L952-9. doi: 10.1152/ajplung.1999.277.5.L952.
PubMed 10564180Garcia-Macedo R, Sanchez-Munoz F, Almanza-Perez JC, Duran-Reyes G, Alarcon-Aguilar F, Cruz M. Glycine increases mRNA adiponectin and diminishes pro-inflammatory adipokines expression in 3T3-L1 cells. Eur J Pharmacol. 2008 Jun 10;587(1-3):317-21. doi: 10.1016/j.ejphar.2008.03.051. Epub 2008 Apr 8.
PubMed 18499099Contreras-Nunez E, Blancas-Flores G, Cruz M, Almanza-Perez JC, Gomez-Zamudio JH, Ventura-Gallegosc JL, Zentella-Dehesa A, Roberto-Lazzarini, Roman-Ramos R, Alarcon-Aguilar FJ. Participation of the IKK-alpha/beta complex in the inhibition of the TNF-alpha/NF-kappaB pathway by glycine: Possible involvement of a membrane receptor specific to adipocytes. Biomed Pharmacother. 2018 Jun;102:120-131. doi: 10.1016/j.biopha.2018.03.048. Epub 2018 Mar 22.
PubMed 29550635
Study at a glance
From the registry record, last updated by the sponsor on 25 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Randomized, Placebo-controlled Clinical Trial Evaluating the Efficacy and Safety of Glycine and Magnesium+Thiamine Supplements, Alone or Combined, Administered for 6 Months to Patients With Primary Ciliary Dyskinesia
- ClinicalTrials.gov ID
- NCT06959251
- Acronym / sponsor ID
- C16-24
- Conditions
- Primary Ciliary Dyskinesia
- Keywords
- Primary ciliary dyskinesia, Glycine, Magnesium, Lung function, thiamine, benfotiamine
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Instituto Nacional de Enfermedades RespiratoriasOther government
- Study start
- 2 Oct 2025 (actual)
- Primary completion
- Mar 2028 (estimated)
- Study completion
- Mar 2028 (estimated)
- First posted
- 6 May 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
- Patients with primary ciliary dyskinesia (PCD) have trouble with clearing their bronchi from mucus, which in the long-term may produce severe damage to the lungs. Currently, there is no specific treatment for PCD beyond supportive measures such as airway hydration and postural drainage.
- Glycine is an amino acid with anti-inflammatory properties that proved to be beneficial in another disease with problematic airway clearance, cystic fibrosis.
- Magnesium participates in many crucial chemical reactions, including some that might favor fluidification and mobilization of mucus. Thiamine (vitamin B1) co-participates with magnesium in some mitochondrial enzymatic reactions occurring in the citric acid cycle.
- Thus, oral supplements of glycine and magnesium+thiamine might improve symptoms and lung function of patients with PCD, and these effects may even be better if these supplements are combined.
- In this study, in addition to their usual care, patients with PCD will receive for 6 months one of the following treatments: 1) an oral supplement of 0.5 g/kg/day glycine, 2) an oral supplement of up to 400 mg/day elementary magnesium plus up to 10 mg/day thiamine, according to the subject's age, 3) glycine plus magnesium+thiamine supplements, as described, or 4) a placebo, which is an inert substance. All treatments will be administered as a whitish powder contained in similar bottles.
- The investigators will evaluate whether glycine and/or magnesium+thiamine reduce exacerbations of the disease, improve pulmonary function and quality of life, and reduce some pro-inflammatory compounds measured in saliva.
Detailed description
Background Primary ciliary dyskinesia (PCD) is characterized by ciliary dysfunction causing mucus accumulation in the airways that favors recurrent infections and bronchiectasis. Apart from general airway clearance, few therapeutic alternatives exist for PCD, and these are usually derived from experiences obtained from other lung diseases such as cystic fibrosis. Among the few clinical trials focused on PCD, the use of azithromycin for 6 months decreased the number of respiratory exacerbations, but with little or no impact on lung function or quality of life. Likewise, although useful in cystic fibrosis, inhalation of hypertonic saline and oral administration of N-acetylcysteine did not improve respiratory symptoms in patients with PCD. Therefore, it is urgent to find therapeutic approaches that prevent respiratory exacerbations, improve quality of life and, ideally, improve lung function. A lot of scientific literature supports the potential beneficial effect of glycine and/or magnesium+thiamine supplements in patients with PCD, as described below. Thus, in this study the investigators will evaluate the effect of glycine and magnesium+thiamine supplementation, alone or combined, in patients with PCD.
Characteristics of glycine Glycine is a non-essential and the simplest amino acid. Physically, it is a whitish powder with a sweet taste, soluble in water and relatively inexpensive (approximately $27 dollars per kg). Aside from participating in protein composition, glycine is an agonist for its own specific receptors (GlyR), which are chloride channels that cause membrane hyperpolarization. In excitable cells such as neurons, glycine is an inhibitory neurotransmitter, while in other cells such as Kupffer cells, alveolar macrophages and neutrophils, this amino acid reduces the sensitivity to proinflammatory stimuli. This stabilizing effect on inflammatory cells has been corroborated in several studies. For example, glycine decreases the expression and levels of tumor necrosis factor (TNF)-α and IL-6 in mouse adipose tissue and prevents the production of TNF-α and superoxide anion in lipopolysaccharide-stimulated alveolar macrophages, as well as TNF-α and IL-6 in 3T3-L1 cells, probably through the inhibition of IKK-α/β and, therefore, of NF-kB phosphorylation. In animal models of endotoxic shock, glycine protects from structural damage and decreases neutrophilic inflammation and proinflammatory cytokine production, probably through inhibition of NF-kB and NLRP3, as well as restoration of NRF2. Recently, in a controlled, crossover clinical trial the investigators administered 0.5 g/kg/day of glycine orally for 8 weeks to children with cystic fibrosis (Vargas et al. BMC Pulm Med 2017;17(1):206. doi: 10.1186/s12890-017-0528-x). This study demonstrated that glycine induced an improvement in clinical and spirometric variables, as well as a decrease in serum TNF-α and a trend towards a decrease in IL-6 and G-CSF. In this and many other studies, oral glycine was virtually devoid of adverse effects.
Possible role of magnesium and thiamine in PCD Epidemiological studies have shown that hypomagnesemia is highly prevalent in the general population, even among self-reported healthy individuals, being as high as 30%. This can be explained by several factors, including Western-type diet, decreased concentration of magnesium in vegetables, use of medications that decrease the intestinal absorption of magnesium or favor its renal elimination, and genetic variants of magnesium transport proteins. Therefore, in patients with PCD, it is expected that at least a similar percentage have a magnesium deficiency. In humans, magnesium is an indispensable element for the proper functioning of at least 300 enzymes involved in vital processes, including those involved in relevant intracellular signaling pathways, for example, kinases (which phosphorylate substrates from ATP-Mg2+), adenylate cyclase (which generates the second messenger cyclic AMP) and G proteins (key GTPases in intracellular signaling of many receptors). Therefore, a relative magnesium deficiency could affect the function of virtually any tissue. In addition, it has been shown that the activity of exogenous rhDNase or endogenous DNases require magnesium in the microenvironment. On the other hand, magnesium is an indispensable cofactor for ATP (ATP-Mg2+) to be utilized by the ATPase domain of dynein and to generate the ciliary beating movement. Therefore, magnesium is important also for mucous fluidification and ciliary functioning. Finally, one of the most relevant metabolic pathways where magnesium is essential is the citric acid cycle, which is the main energy (ATP) generator in the mitochondria, since it is a cofactor of pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase and branched-chain keto amino acid dehydrogenase, as well as other related enzymes such as transketolase and 2-hydroxyacyl CoA lyase. It is important to note that in addition to magnesium, all these enzymes also require thiamine diphosphate, so that the deficiency of either cofactor (magnesium and thiamine) leads to mitochondrial dysfunction. This is particularly relevant in PCD because proper mitochondrial function is essential for the formation and functioning of cilia.
Hypothesis
- In patients with PCD, glycine or magnesium+thiamine supplementation for 6 months will be associated with a 25% decrease in the number of respiratory exacerbations compared to placebo.
- In patients with PCD, combined glycine and magnesium+thiamine supplements for 6 months will be associated with a 50% decrease in the number of respiratory exacerbations compared to placebo.
Major objective To evaluate the effect of glycine and magnesium+thiamine supplements, alone or combined, administered for 6 months to patients with PCD on the number of respiratory exacerbations.
Secondary objectives
To evaluate the effect of glycine and magnesium+thiamine supplements, alone or combined, administered for 6 months to patients with PCD on:
- Quality of life (questionnaire of the Spanish version of the QOL-PCD, as well as some questions on possible side effects).
- Growth and development (weight-for-height, height-for-age, BMI).
- Peripheral oxygen saturation (SpO2).
- Pulmonary function tests (nasal nitric oxide, oscillometry, multiple breath nitrogen washout, spirometry, 6-min walking test).
- Biomarkers in saliva (IL-1β, IL-6, IL-8, TNF-α, MPO).
Description of the study The study will be carried out at the Instituto Nacional de Enfermedades Respiratorias (INER), located in Mexico City. Once an informed consent is signed by patients or their legal guardians, participants will be randomly allocated to one of four study arms: 1) glycine, 2) magnesium+thiamine, 3) glycine and magnesium+thiamine, 4) placebo. Glycine will be administered at a dose of 0.5 g/kg/day, up to a maximum of 25 g/day. The dose of magnesium will be 8 mg/kg/day of elementary magnesium administered as magnesium citrate, up to a maximum of 400 mg/day. The dose of thiamine will be 0.2 mg/kg/day administered as benfotiamine, up to a maximum of 10 mg/day. Patients or their legal guardians will be asked to fill out an online symptom questionnaire every week. At the initial visit and every 2 months the following maneuvers will be performed: inquiry about pulmonary exacerbations; weight and height measurements; physical examination; pulse oximetry; saliva sampling for measuring IL-1β, IL-6, IL-8, TNF-α, myeloperoxidase (MPO) and albumin; nasal nitric oxide measurement; basal oscillometry; multiple breath nitrogen washout test; basal spirometry; post-salbutamol oscillometry and spirometry, 6-min walk test. In each visit, except for the final visit, a 500 g plastic bottle with a mixture of glycine, magnesium+thiamine, and/or placebo (sugar glass) powders, according to their assigned group, will be given to the patient or to the person at charge. All bottles will be identical in appearance.
Sample size Due to feasibility reasons, the investigators consider that the number of participants in each of the four groups will be n=15 (total n=60 patients).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 4
- Model description
- Four arms, parallel design, placebo controlled.
| Arm | Type | Receives |
|---|---|---|
| Glycine | Experimental | Dietary Supplement: GlycinePatients will receive for 6 months an oral supplement of 0.5 g/kg/day glycine, up to 25 g/day, divided in three daily intakes. |
| Magnesium+thiamine | Experimental | Dietary Supplement: Magnesium+thiaminePatients will receive for 6 months an oral supplement of up to 400 mg/day, according to age, of elementary magnesium (formulated as magnesium citrate) plus up to 10 mg/day of thiamine (formulated as benfotiamine), divided in three daily intakes. |
| Glycine plus magnesium+thiamine | Experimental | Dietary Supplement: Glycine, Dietary Supplement: Magnesium+thiaminePatients will receive for 6 months oral supplements of glycine and magnesium+thiamine, as described. |
| Placebo | Placebo comparator | Other: PlaceboPatients will receive for 6 months placebo (sugar glass), in a similar daily amount as in experimental arms, and divided in three daily intakes. |
Who may qualify
- Ages
- 5 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (7 listed)
- Any sex.
- Age of 5 years or more.
- Diagnosis of primary ciliary dyskinesia (PCD) established according to international recommendations (Shapiro et al. Am J Respir Crit Care Med 2018;197(12):e24-e39, and Shapiro et al. Ped Pulmonol 2016;51:115-132).
- Without respiratory exacerbations of PCD in the previous 30 days.
- Without acute respiratory infection in the previous 30 days.
Key exclusion criteria (3 listed)
- 1. Participation in other research protocol involving therapeutic measures.
- 1. None.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| GlycinePatients will receive for 6 months an oral supplement of 0.5 g/kg/day glycine, up to 25 g/day, divided in three daily intakes. | Dietary supplement | Glycine, Glycine plus magnesium+thiamine |
| Magnesium+thiaminePatients will receive for 6 months an oral supplement of up to 400 mg/day, according to age, of elementary magnesium (formulated as magnesium citrate) plus up to 10 mg/day of thiamine (formulated as benfotiamine), divided in three daily intakes. | Dietary supplement | Glycine plus magnesium+thiamine, Magnesium+thiamine |
| PlaceboPatients will receive for 6 months placebo (sugar glass), in a similar daily amount as in experimental arms, and divided in three daily intakes. | Other | Placebo |
Primary outcome
Number of respiratory exacerbations
Time frame: 6 months
A respiratory exacerbation will be defined as: 1) any increase in respiratory symptoms that motivated the initiation of antibiotic therapy, or 2) a 10% or more decrease in FEV1 with respect to the FEV1 value at recruitment. A blinded pediatric pulmonologist will review all cases to corroborate whether a suspected episode was indeed a respiratory exacerbation.
26 secondary outcomes
Quality of life-Primary ciliary dyskinesia questionnaire (QOL-PCD)
Time frame: 6 months
Weight-for-height
Time frame: 6 months
Height-for-age
Time frame: 6 months
SpO2
Time frame: 6 months
Body mass index
Time frame: 6 months
Nasal nitric oxide
Time frame: 6 months
R5
Time frame: 6 months
R20
Time frame: 6 months
R5-R20
Time frame: 6 months
(R5-R20)/R5
Time frame: 6 months
X5
Time frame: 6 months
X20
Time frame: 6 months
Frequency of resonance (Fres)
Time frame: 6 months
Area of reactance (AX)
Time frame: 6 months
Multiple breath nitrogen washout
Time frame: 6 months
FVC
Time frame: 6 months
FEV1
Time frame: 6 months
FEV1/FVC
Time frame: 6 months
Response to bronchodilator (oscillometry)
Time frame: 6 months
Response to bronchodilator (spirometry)
Time frame: 6 months
6-minute walk test
Time frame: 6 months
IL-1beta in saliva
Time frame: 6 months
IL-6 in saliva
Time frame: 6 months
IL-8 in saliva
Time frame: 6 months
TNF-alpha in saliva
Time frame: 6 months
MPO in saliva
Time frame: 6 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 25 Nov 2025.
- Background: PubMed 32284045Piatti G, De Santi MM, Farolfi A, Zuccotti GV, D'Auria E, Patria MF, Torretta S, Consonni D, Ambrosetti U. Exacerbations and Pseudomonas aeruginosa colonization are associated with altered lung structure and function in primary ciliary dyskinesia. BMC Pediatr. 2020 Apr 13;20(1):158. doi: 10.1186/s12887-020-02062-4.
- Background: PubMed 35984413Sagel SD, Kupfer O, Wagner BD, Davis SD, Dell SD, Ferkol TW, Hoppe JE, Rosenfeld M, Sullivan KM, Tiddens HAWM, Knowles MR, Leigh MW. Airway Inflammation in Children with Primary Ciliary Dyskinesia. Ann Am Thorac Soc. 2023 Jan;20(1):67-74. doi: 10.1513/AnnalsATS.202204-314OC.
- Background: PubMed 22648717Gontijo-Amaral C, Guimaraes EV, Camargos P. Oral magnesium supplementation in children with cystic fibrosis improves clinical and functional variables: a double-blind, randomized, placebo-controlled crossover trial. Am J Clin Nutr. 2012 Jul;96(1):50-6. doi: 10.3945/ajcn.112.034207. Epub 2012 May 30.
- Background: PubMed 29246256Vargas MH, Del-Razo-Rodriguez R, Lopez-Garcia A, Lezana-Fernandez JL, Chavez J, Furuya MEY, Marin-Santana JC. Effect of oral glycine on the clinical, spirometric and inflammatory status in subjects with cystic fibrosis: a pilot randomized trial. BMC Pulm Med. 2017 Dec 15;17(1):206. doi: 10.1186/s12890-017-0528-x.
- Background: PubMed 32380069Kobbernagel HE, Buchvald FF, Haarman EG, Casaulta C, Collins SA, Hogg C, Kuehni CE, Lucas JS, Moser CE, Quittner AL, Raidt J, Rosthoj S, Sorensen AL, Thomsen K, Werner C, Omran H, Nielsen KG. Efficacy and safety of azithromycin maintenance therapy in primary ciliary dyskinesia (BESTCILIA): a multicentre, double-blind, randomised, placebo-controlled phase 3 trial. Lancet Respir Med. 2020 May;8(5):493-505. doi: 10.1016/S2213-2600(20)30058-8.
- Background: PubMed 28232410Paff T, Daniels JM, Weersink EJ, Lutter R, Vonk Noordegraaf A, Haarman EG. A randomised controlled trial on the effect of inhaled hypertonic saline on quality of life in primary ciliary dyskinesia. Eur Respir J. 2017 Feb 23;49(2):1601770. doi: 10.1183/13993003.01770-2016. Print 2017 Feb.
- Background: PubMed 3345250Jensen T, Kharazmi A, Schiotz PO, Nielsen H, Stenvang Pedersen S, Stafanger G, Koch C, Hoiby N. Effect of oral N-acetylcysteine administration on human blood neutrophil and monocyte function. APMIS. 1988 Jan;96(1):62-7. doi: 10.1111/j.1699-0463.1988.tb05269.x.
- Background: PubMed 11917096Jentsch TJ, Stein V, Weinreich F, Zdebik AA. Molecular structure and physiological function of chloride channels. Physiol Rev. 2002 Apr;82(2):503-68. doi: 10.1152/physrev.00029.2001.
- Background: PubMed 19738917Van den Eynden J, Ali SS, Horwood N, Carmans S, Brone B, Hellings N, Steels P, Harvey RJ, Rigo JM. Glycine and glycine receptor signalling in non-neuronal cells. Front Mol Neurosci. 2009 Aug 20;2:9. doi: 10.3389/neuro.02.009.2009. eCollection 2009.
- Background: PubMed 10926563Wheeler MD, Rose ML, Yamashima S, Enomoto N, Seabra V, Madren J, Thurman RG. Dietary glycine blunts lung inflammatory cell influx following acute endotoxin. Am J Physiol Lung Cell Mol Physiol. 2000 Aug;279(2):L390-8. doi: 10.1152/ajplung.2000.279.2.L390.
- Background: PubMed 18930730Alarcon-Aguilar FJ, Almanza-Perez J, Blancas G, Angeles S, Garcia-Macedo R, Roman R, Cruz M. Glycine regulates the production of pro-inflammatory cytokines in lean and monosodium glutamate-obese mice. Eur J Pharmacol. 2008 Dec 3;599(1-3):152-8. doi: 10.1016/j.ejphar.2008.09.047. Epub 2008 Oct 9.
- Background: PubMed 19864106Almanza-Perez JC, Alarcon-Aguilar FJ, Blancas-Flores G, Campos-Sepulveda AE, Roman-Ramos R, Garcia-Macedo R, Cruz M. Glycine regulates inflammatory markers modifying the energetic balance through PPAR and UCP-2. Biomed Pharmacother. 2010 Oct;64(8):534-40. doi: 10.1016/j.biopha.2009.04.047. Epub 2009 Oct 17.
- Individual participant dataSharing planned: Yes. Data will be available upon reasonable request for research purposes.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Mario H. Vargas, MSc principal investigator
5556665868
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Glycine and Magnesium+thiamine in people with Primary Ciliary Dyskinesia, run by Instituto Nacional de Enfermedades Respiratorias at 1 site in Mexico.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 25 Nov 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Mexico. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mario H. Vargas, MSc (5556665868, mhvargasb@yahoo.com.mx), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of respiratory exacerbations (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06959251, which also lists 43 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Nov 2025.