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UndernutritionMIDIWANCT02962089

Microbiota and Protein-energy Wasting (MIDIWA)

A study testing Branched chain amino acids (BCAA) in people with Undernutrition, run by University Hospital, Geneva at 5 sites in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Oral supplementation with branched chain amino acids (BCAA) increases the levels of circulating BCAA, stimulates BCAA uptake in muscles, and decreases amino acid release from muscle, eventually promoting muscle anabolism. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Undernutrition
What is being tested?
Branched chain amino acids (BCAA)
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
37 participants
Where
5 sitesSwitzerland
Study dates
Aug 2016to Aug 2019
Phase
Interventional
Are there results?
None posted in the registry

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 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years.
  • Maintenance hemodialysis for at least 3 months.
  • Fasting predialysis plasma albumin < 38 g/l in the absence of any known acute infection during the last 2 weeks or body weight loss > 5% of estimated dry body weight over 3 months
  • Dietary intakes (24h dietary recall) between 20-30 kcal/kg/d and < 1 g protein/kg/d on one occasion, during screening. These intakes will not include the intake of oral nutritional supplements, as intakes below 20 kcal/kg/d request artificial nutrition
  • Absence of any systematic antibiotic treatment for an acute infection in the month preceding the inclusion

Who cannot join

  • Known psychiatric or cognitive disorder, precluding protocol compliance.
  • Life expectancy below 1 year.
  • Inadequate dialysis (Kt/V<1.2 on 3 consecutive occasions, for HD patients only), if applicable.
  • Enteral or parenteral nutrition.
  • Drugs or oral nutritional supplements containing fibers since ≤ 1 month.
  • Known reasons for decreased plasma albumin levels as liver failure or exudative enteropathy.
Show all 9Show fewer
  • Drugs influencing body composition, ≤ 1 month : systemic corticosteroids, anabolic drugs as insulin or testosterone, post-menopausal hormone therapy, injectable contraceptives.
  • Known endocrinological disorders potentially leading to hypo- or hypermetabolism, untreated or treated since ≤ 1 month : disorders of thyroid gland, adrenal glands...
  • Pregnancy and breast-feeding.

Trial locations and contacts

5 sites in 1 country.

5 sites in 1 country

Switzerland5 sites
  • Geneva University Hospital

    Geneva, 1205

  • Champel clinic

    Geneva, 1206

  • Cécil clinic

    Lausanne, Canton of Vaud, 1003

  • Lausanne University Hospital

    Lausanne, Canton of Vaud, 1011

  • Hospital of Sion

    Sion, Valais, 1951

Other trials in Switzerland

About this study

Official title: Do Branched Chain Amino Acids Counteract Protein Energy Wasting Through Gut Microbiota Changes in Hemodialysis Patients ?

Oral supplementation with branched chain amino acids (BCAA) increases the levels of circulating BCAA, stimulates BCAA uptake in muscles, and decreases amino acid release from muscle, eventually promoting muscle anabolism. However, uptake of oral BCAA by muscle is not complete, pointing out that non-muscular tissues, as the splanchnic bed and gut microbiota, may play a role in BCAA metabolism.

This protocol aims at studying the impact of protein-energy wasting (PEW) and of refeeding with branched chain amino acids (BCAA), on gut barrier including gut microbiota, in chronic hemodialysis (HD) patients. The investigators speculate that:

  1. HD patients with PEW have altered composition and function of gut microbiota, increased permeability of epithelial gut barrier, increased systemic inflammation but decreased fecal immunoglobulin A (IgA), and a dysbalance of plasma appetite mediators in favor of anorexigenic mediators, compared to HD patients without PEW, non dialyzed patients with chronic kidney disease and well-nourished non obese subjects,
  2. BCAA supplementation of HD patients with PEW reverses these changes, thereby improving nutritional state, physical function, quality of life and resistance to infections.
Read the detailed description

General description :

This protocol is multicenter (University Hospitals of Geneva (HUG), Lausanne University Hospital (CHUV), Hospital of Sion (HVS), dialysis center of the Champel clinic in Geneva and dialysis center of the Cécil clinic in Lausanne) and encompasses two parts, a cross-sectional and a longitudinal study:

  1. Cross-sectional study: It is performed to differentiate the respective impact of uremia and protein-energy wasting (PEW) on gut barrier and gut microbiota. It will compare gut barrier of hemodialysis (HD) patients with PEW, with gut barrier of age-matched HD well-nourished patients, non dialyzed patients with chronic kidney disease (CKD), and healthy non obese volunteers (10 in each group). This study part is essential for interpretation of the changes occurring in the longitudinal study.
  2. Longitudinal double blind randomized crossover study: HD patients with PEW (36 patients), receive, in a randomized double-blind order, either BCAA or an isocaloric isonitrogenous placebo for 4 months each, with a wash-out period of 1 month.

Randomization :

  1. Cross-sectional study: No randomization will be performed. HD patients without PEW, non dialyzed patients with CKD and healthy non obese volunteers will be included if matched for gender and age with the included HD patients with PEW. Age-matching will allow a discrepancy of +/- 5 years compared to the HD patient.
  2. Longitudinal study: Sequence assignment will be randomized separately in each center to ensure an equal percentage of each sequence in both centers. For this purpose, the investigators will generate 2 lists of randomization with the method of randomly permuted blocks with random block sizes of 2 and 4.

Recruitment :

Patients will be recruited among the outpatients of the Nephrology Divisions or Services of the HUG, CHUV, HVS and Champel and Cécil clinics. Healthy volunteers will be recruited among hospital staff or their relatives.

Inclusion Criteria :

  1. HD patients with PEW
  • Age ≥ 18 years.
  • Maintenance HD for at least 3 months.
  • Fasting predialysis plasma albumin < 38 g/l in the absence of an known acute infection during the last 2 weeks or body weight loss > 5% of estimated dry body weight over 3 months
  • Dietary intakes (24h dietary recall) between 20-30 kcal/kg/d and < 1 g protein/kg/d on one occasion, during screening. These intakes will not include the intake of oral nutritional supplements, as intakes below 20 kcal/kg/d request artificial nutrition.
  • Absence of any systematic antibiotic treatment for an acute infection in the month preceding the inclusion.
  1. HD patients without PEW
  • Patients matched for age and gender to HD patients with PEW.
  • Maintenance HD for at least 3 months.
  • Fasting predialysis plasma albumin ≥ 40 g/l, in the absence of any known acute infection during the last 2 weeks
  • Dietary intakes (24h dietary recall) > 30 kcal/kg/d and > 1.2 g protein/kg/d, once during screening.
  • Absence of any systematic antibiotic treatment for an acute infection in the month preceding the inclusion.
  1. Non dialysed patients with chronic kidney disease stage 4
  • Patients matched for age and gender to HD patients with PEW.
  • Chronic kidney disease, stage 4 or 5, not requiring HD.
  • Fasting predialysis plasma albumin ≥ 40 g/l, in the absence of any known acute infection during the last 2 weeks
  • Dietary intakes (24h dietary recall) > 30 kcal/kg/d once during screening.
  • Absence of any systematic antibiotic treatment for an acute infection in the month preceding the inclusion.
  1. Healthy non obese volunteers
  • Subjects matched for age and gender to HD patients with PEW.
  • Body mass index < 30 kg/m2
  • Absence of chronic disease potentially leading to wasting or cachexia.
  • Absence of plasma C-reactive protein > 50 mg/l in the last 2 weeks or known acute infection.
  • Absence of any systematic antibiotic treatment for an acute infection in the month preceding the inclusion.
Conditions
Undernutrition
Being tested
Branched chain amino acids (BCAA), Placebo
Keywords
Protein-energy wasting, Hemodialysis patients, Microbiota, Branched chain amino acids, Undernutrition, Malnutrition, Renal failure, Dialysis, Protein, Appetite, Body composition, Energy expenditure
Medical subject headings
Malnutrition, Renal Insufficiency

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Branched chain amino acids (BCAA)Dietary supplement

  • PlaceboDietary supplement

Study groups in NCT02962089
Study groupRoleWhat they receive
PlaceboPlacebo comparatorIsocaloric isonitrogenous placebo for 4 months (7g, twice daily)
Receives: Dietary Supplement: Placebo
Branched chain amino acids (BCAA)Active comparatorBCAA mixture for 4 months (7g, twice daily)
Receives: Dietary Supplement: Branched chain amino acids (BCAA)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Gut microbiota composition by 16-S high throughput sequencing

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  2. Gut microbiota function by 16-S high throughput sequencing

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

Secondary outcomes (20)
  1. Epithelial gut barrier function by fasting level of plasma glucagon-like peptide-2

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  2. Epithelial gut barrier function by fasting level of plasma lipopolysaccharide

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  3. Intestinal immunity by level of fecal IgA

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  4. Systemic inflammation by fasting level of plasma interleukin 10

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  5. Systemic inflammation by fasting level of plama interleukin 6

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  6. Systemic inflammation by fasting level of plama tumor necrosis factor alpha

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  7. Appetite by fasting level of plasma cholecystokinin

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  8. Appetite by fasting level of plasma leptin

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  9. Appetite by fasting level of plasma peptide YY

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  10. Appetite by fasting level of plasma glucagon-like peptide-1

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  11. Appetite by fasting level of plasma neuropeptide Y

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  12. Appetite by fasting level of plasma ghrelin

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  13. Appetite by fasting level of plasma endocannabinoids

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  14. Calorie and protein intakes by 3-day food diary

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  15. Body composition by dual-energy x-rax absorptiometry (DEXA)

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  16. Resting energy expenditure (REE) by indirect calorimetry

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  17. Physical activity level by 7-day pedometry

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  18. Handgrip strength by dynamometer

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  19. Quality of life score by Short Form Health Survey (SF-36)

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)

  20. Body composition by bioelectrical impedance analysis

    Measured: Changes between baseline and end of each treatment (i.e.changes between Month 0,2, and Month 4 and between Month 5,7 and Month 9)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Nov 2016 (estimated)
  2. Study startAug 2016
  3. Primary completionAug 2019
  4. Study completionAug 2019

Resources

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
Supportive care
Allocation
Randomised
Intervention model
Crossover
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
37 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02962089
Sponsor's protocol ID
CER 13-239
Acronym
MIDIWA
Status last verified
Apr 2021
First submitted
23 Aug 2016
Last updated
28 Apr 2021
Results posted
No
Data monitoring committee
Yes
Individual data sharing
No

Publications

  • Genton L, Pruijm M, Teta D, Bassi I, Cani PD, Gaia N, Herrmann FR, Marangon N, Mareschal J, Muccioli GG, Stoermann C, Suriano F, Wurzner-Ghajarzadeh A, Lazarevic V, Schrenzel J. Gut barrier and microbiota changes with glycine and branched-chain amino acid supplementation in chronic haemodialysis patients. J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1527-1539. doi: 10.1002/jcsm.12781. Epub 2021 Sep 18.

    PubMed 34535959
  • Genton L, Teta D, Pruijm M, Stoermann C, Marangon N, Mareschal J, Bassi I, Wurzner-Ghajarzadeh A, Lazarevic V, Cynober L, Cani PD, Herrmann FR, Schrenzel J. Glycine increases fat-free mass in malnourished haemodialysis patients: a randomized double-blind crossover trial. J Cachexia Sarcopenia Muscle. 2021 Dec;12(6):1540-1552. doi: 10.1002/jcsm.12780. Epub 2021 Sep 14.

    PubMed 34519439

Questions about this trial

What is this clinical trial studying?

A study testing Branched chain amino acids (BCAA) in people with Undernutrition, run by University Hospital, Geneva at 5 sites in Switzerland.

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 5 inclusion and 9 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: finished, as of the sponsor's last update on 28 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 5 sites in Switzerland. 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?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Gut microbiota composition by 16-S high throughput sequencing (time frame: Changes between baseline and end of each treatment (i.e.changes between Month 0 and Month 4 and between Month 5 and Month 9)). The study lists 2 primary outcomes in all. 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 NCT02962089, which also lists 2 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 28 Apr 2021.

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