PeriodontitisPhase 3NCT06726876
Therapeutic Effect of Manuka Honey Oral Rinse in Periodontitis Patients Undergoing Hemodialysis
A Phase 3 study testing Manuka honey oral rinse. and Normal saline rinses. in people with Periodontitis and Hemodialysis, run by Ain Shams University at 1 site in Egypt.
Trial summary
Chronic Kidney Disease (CKD) has a strong association with chronic periodontitis, an oral disease causing tooth loss linked to inflammation and malnutrition. While periodontitis affects 12.7% of the general population, its prevalence can rise to 39% in certain racial groups, and a dose-response relationship exists… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Periodontitis, Hemodialysis
- What is being tested?
- Manuka honey oral rinse. and Normal saline rinses.
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 150 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Oct 2024to 30 Dec 2025
- Phase
- Phase 3
- 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 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Both genders, aged above 18 years.
- All patients must be clinically diagnosed of ESRD undergoing hemodialysis.
- All patients must have a periodontal disease.
- Patients must be able to make reliable decision or communications.
Who cannot join
- Smoking, Alcohol.
- Patient with history of any serious illness as malignancy, who undergo kidney transplant.
- Patients with any autoimmune disease.
- Vulnerable groups such as pregnant females, prisoners, mentally and physically handicapped individuals.
- Known hypersensitivity or severe adverse effects to the treatment drugs or to any ingredient of their preparation.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Egypt1 site, 1 recruiting
- Recruiting
Benha hospital
Banhā
Asmaa Bakr elshaf3y, 01000093885, Asmaa.AbdAlRaouf@gu.edu.eg
About this study
Chronic Kidney Disease (CKD) has a strong association with chronic periodontitis, an oral disease causing tooth loss linked to inflammation and malnutrition. While periodontitis affects 12.7% of the general population, its prevalence can rise to 39% in certain racial groups, and a dose-response relationship exists with CKD. End Stage Renal Disease (ESRD) patients show a prevalence of periodontitis ranging from 29% to 85.6%. Uremia, immunosuppression, and vitamin D deficiency are suggested factors in the etiology of periodontitis in CKD patients, with uremic toxins potentially altering the oral ecosystem.
Periodontitis involves bacterial biofilm and Gram-negative anaerobes as primary etiological factors. The main treatment goal is to reduce periodontal pathogens and control inflammation, with non-surgical periodontal therapy (NSPT) being the standard. Although various adjuncts like antibiotics and antiseptics are suggested, recent guidelines only recommend certain locally administered agents and systemic antibiotics for specific groups due to increasing bacterial resistance.
Read more
Alternative treatments like honey have gained interest, particularly Manuka honey, known for its antibacterial properties against antibiotic-resistant bacteria. This honey's effectiveness is due to its high sugar concentration, low pH, and formation of hydrogen peroxide. Manuka honey's unique component, methylglyoxal (MGO), is a potent bactericide, virucide, and fungicide, linked to its Non-Peroxide Activity (NPA) and Unique Manuka Factor (UMF) rating. MGO also has immunomodulatory effects beneficial for wound healing and tissue regeneration.
Previous studies show Manuka honey as a promising adjunct in NSPT, improving outcomes significantly without adverse effects. Ongoing research aims to evaluate its effects in ESRD patients on hemodialysis, focusing on clinical attachment levels, other periodontal parameters, and FGF 21 levels in gingival crevicular fluid.
Read the detailed description
Chronic Kidney Disease (CKD) is associated with a high prevalence of chronic periodontitis, an infectious oral disease that causes tooth loss and is linked to inflammation and malnourishment [1]. The frequency of periodontitis is 12.7% in the general population, according to recent epidemiological studies [2], but it can reach as high as 39% in certain racial groups [3, 4], and there is a dose-response relationship with CKD [5]. The prevalence of periodontitis in End Stage Renal Disease (ESRD) has been reported in smaller studies to range from 29 to 85.6% [6, 7, 8]. It has been proposed that uremia and associated immunosuppression, as well as vitamin D deficiency, play a role in the etiology of periodontitis in CKD [5, 9, 10].
Uremic toxins may potentially alter the oral ecosystem (hydrolysis of urea results in alkaline pH) promoting the growth of periodontal pathogens, in a similar manner to the demonstrated uremia-related changes in the gut environment [11, 12]. Studies using microbiological methods of limited scope have shown that ESRD individuals with periodontitis have increased levels of periodontal pathogens as compared to non-CKD controls [13].
Periodontitis is a chronic inflammatory disease affecting the teeth's supporting apparatus. Bacterial biofilm and the associated periodontal pathogenic bacteria, mainly Gram-negative anaerobes, are the main etiological factor of the disease [14].
The main goal of periodontal treatment is to reduce the number of periodontal pathogens and arrest the inflammatory process. The contemporary gold treatment standard is non-surgical periodontal therapy (NSPT), which involves scaling and root planning using manual and machine-driven (sonic or ultrasonic) instruments [15].
Various systemically administered and locally delivered adjuncts to NSPT have been suggested, including systemic and local antibiotics, antiseptics, probiotics, lasers, and photodynamic treatment. However, the latest guidelines on the treatment of periodontitis stage I-III do not support the use of adjuncts. The exception in terms of open recommendations is given for locally administered sustained-release chlorhexidine and antibiotics and the use of systemic antibiotics in specific patient groups [15].
The fact that bacteria are becoming increasingly resistant to antibiotics and antiseptics has shifted the interest of medicine to alternative treatment methods against which bacterial resistance cannot be developed. This approach includes using honey, which is increasingly used in medicine. Since the 1990s, when the first studies appeared on the therapeutic effects of honey, particular interest has been focused on its antibacterial properties against infections and antibiotic-resistant bacteria. This effect is consequential mainly of the high sugar concentration of honey, its low pH value, and the formation of hydrogen peroxide that occurs in the enzymatic breakdown of glucose by the glucose oxidase enzyme [16]. Contemporary research on the effects of honey focuses predominantly on one specific honey type, leading to the medicinal use of Manuka honey due to its antibacterial properties [17]. This is an endemic type of honey produced by bees in Australia and New Zealand from the flowers of the plant Leptospermum scoparium [18].
The concentration of hydrogen peroxide in Manuka honey is lower than in other types of honey [19]. The specific antibacterial activity in Manuka honey is based on methylglyoxal (MGO), a compound proven to be a very efficient bactericide, virucide, and fungicide. Furthermore, Manuka honey is highly effective against antibiotic-resistant bacteria [20].
The antibacterial potency of Manuka honey was found to be related to its Non-Peroxide Activity (NPA), trademarked as Unique Manuka Factor (UMF) rating, a classification system which reflects the equivalent concentration of phenol (%, w/v) required to produce the same antibacterial activity as honey, and it is correlated with the methylglyoxal and total phenols content [21]. In addition to its antimicrobial properties, published literature suggests that MGO also has immunomodulatory effects which may positively impact wound healing and tissue regeneration [22,23].
A previous pilot study indicated a promising potential of Manuka honey as an adjunct in NSPT. Despite the improvement in outcomes appearing modest in absolute terms, it was statistically significant for all follow-up time points, indicating the potential use of Manuka honey as a simple and affordable adjunct to non-surgical periodontal therapy. Furthermore, the product is considered a safe adjunct and no adverse events related to its use were reported during the study period. Encouraging results from this pilot study led to a further randomized clinical study on a larger sample that is currently being performed by our group [24].
Manuka honey oral rinse has not yet been investigated as a possible adjunct to NSPT in ESRD patients on regular hemodialysis. Therefore, this study aims to evaluate the effects of Manuka honey oral rinse on clinical attachment level (CAL) as a primary objective, and other periodontal parameters like (BOP, plaque index), and its effect on the levels of FGF 21 in gingival crevicular fluid as secondary objectives after nonsurgical periodontal treatment in patients with periodontitis.
- Conditions
- Periodontitis, Hemodialysis
- Being tested
- Manuka honey oral rinse., Normal saline rinses.
- Keywords
- Manuka honey, fibroblast growth factor-21, periodontitis, hemodialysis
- Medical subject headings
- Periodontitis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Manuka honey oral rinse.Dietary supplement
Name: Manuka Honey Oral Rinse
Description:
Dosage: Patients will use 20 ml of Manuka honey diluted in 100 ml of purified water.
Administration: Oral rinse, performed 3 times per day.
Instructions: Patients are instructed to rinse their mouths with the solution for a specified duration and avoid swallowing it.
Unique Elements:
Active Ingredient: Manuka honey, known for its unique antibacterial properties due to high levels of methylglyoxal (MGO).
Mechanism of Action: MGO and Non-Peroxide Activity (NPA) contribute to antibacterial potency, effective against antibiotic-resistant bacteria, and potential immunomodulatory effects that aid wound healing and tissue regeneration.
Additional Procedures: Scaling and root debridement, along with the local application of 0.5 ml non-diluted Thyme honey on sites with Probing Pocket Depth (PPD) ≥ 5 mm.
Supplementary Care: Patients receive motivation and detailed oral hygiene instructions (proper tooth brushing technique, flossing, use of inte
Normal saline rinses.Drug
Dosage: Patients will use 20 ml of normal saline.
Administration: Oral rinse, performed 3 times per day.
Instructions: Patients are instructed to rinse their mouths with the saline solution for a specified duration and avoid swallowing it.
Unique Elements:
Control Comparison: Provides a placebo comparison to evaluate the efficacy of the Manuka honey intervention.
Additional Procedures: Scaling and root debridement, along with the local application of 0.5 ml non-diluted Thyme honey on sites with Probing Pocket Depth (PPD) ≥ 5 mm.
| Study group | Role | What they receive |
|---|---|---|
| Control Group | Placebo comparator | Treatment: Normal saline rinse.
Protocol:
Follow the same protocol as the intervention group but using normal saline rinses instead of Manuka honey.
Additional Treatment: Patients will receive scaling and root debridement and locally delivered 0.5 ml non-diluted Thyme honey on sites with PPD ≥ 5 mm.
Supplementary Care: Motivation, oral hygiene instructions (proper tooth brushing technique, flossing, interdental brush, mouthwash usage), scaling, polishing, and root debridement with an ultrasonic scaler and Gracey curettes. Receives: Drug: Normal saline rinses. |
| Intervention Group | Experimental | Treatment: Manuka honey oral rinse.
Protocol:
Applied as an oral rinse based on the Biswal et al. administration protocol.
Patients will have oral rinses (20 ml of Manuka honey diluted in 100 ml of purified water) 3 times per day.
Patients will be instructed not to swallow the Manuka honey oral rinse.
Additional Treatment: Patients will receive scaling and root debridement and locally delivered 0.5 ml non-diluted Thyme honey on sites with PPD ≥ 5 mm.
Supplementary Care: Motivation, oral hygiene instructions (proper tooth brushing technique, flossing, interdental brush, mouthwash usage), scaling, polishing, and root debridement with an ultrasonic scaler and Gracey curettes. Receives: Dietary Supplement: Manuka honey oral rinse. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Clinical Attachment Level (CAL)
Description: Measurement of the attachment level of the periodontal ligament to the tooth surface, indicating the health of periodontal tissues.
Measured: Evaluated at baseline, 3 months, and 6 months post-treatment.
Secondary outcomes (6)
Bleeding on Probing (BOP)
Description: Assessment of bleeding on probing, which is an indicator of inflammation in periodontal tissues.
Measured: Evaluated at baseline, 3 months, and 6 months post-treatment.
Plaque Index
Measurement of the amount of dental plaque on the tooth surface, which is an indicator of oral hygiene.
Measured: Evaluated at baseline, 3 months, and 6 months post-treatment.
Fibroblast Growth Factor 23 (FGF 23) Levels in Gingival Crevicular Fluid (GCF)
Measurement of FGF 23 levels in gingival crevicular fluid, which may reflect tissue response and inflammation levels.
Measured: Evaluated at baseline and at 6 months post-treatment.
Fibroblast Growth Factor 23 (FGF 23) Levels in serum
Measurement of FGF 23 levels in serum, which may reflect tissue response and inflammation levels.
Measured: Evaluated at baseline and at 6 months post-treatment.
Oral Health Impact Profile (OHIP-14) scores
measured on a 5-point Likert scale. Lower scores indicate better oral health-related quality of life (OHRQoL)
Measured: baseline, and 6 months
Serum C-Reactive Protein (CRP)
Serum C-reactive protein (CRP) was measured as a marker of systemic inflammation in patients with end-stage renal failure (ESRF) and periodontitis. Venous blood samples were collected under standardized conditions, and serum was separated by centrifugation. CRP levels were quantified using a validated laboratory assay according to routine clinical laboratory protocols, and results were expressed in milligrams per liter (mg/L).
CRP is an acute-phase protein produced by the liver in response to inflammatory stimuli. In ESRF, CRP levels may be chronically elevated due to uremia and dialysis-related inflammation, while periodontitis represents an additional source of persistent inflammatory burden. Accordingly, CRP in this study was used as an indicator of overall systemic inflammation rather than a disease-specific diagnostic marker. Higher CRP values were interpreted as reflecting increased inflammatory activity and were analyzed in relation to periodontal status and disease severity.
Measured: baseline, 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Dec 2024
- Study start1 Oct 2024
- Primary completion30 Dec 2025 (estimated)
- Study completion30 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for PeriodontitisStudies of the same condition, open and under way.
- More trials run by Ain Shams UniversityThe sponsor's other registered studies.
- 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 3
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind
- Who is masked
- Care provider, Investigator, Outcomes assessor
- Enrolment
- 150 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ain Shams University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Fatma ElSayed, Ain Shams University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06726876
- Sponsor's protocol ID
- R626
- Status last verified
- Dec 2025
- First submitted
- 6 Dec 2024
- Last updated
- 31 Dec 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Abou-Bakr A, Nagi N, Ibrahim M, Alqahtani AS, Hassanein FEA. ADJUNCTIVE MANUKA HONEY ORAL RINSE IN NONSURGICAL PERIODONTAL THERAPY FOR HEMODIALYSIS PATIENTS: A RANDOMIZED CONTROLLED CLINICAL STUDY. J Evid Based Dent Pract. 2026 Sep;26(3):102312. doi: 10.1016/j.jebdp.2026.102312. Epub 2026 May 22.
PubMed 42556897
Study at a glance
From the registry record, last updated by the sponsor on 31 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Therapeutic Effect of Manuka Honey Oral Rinse in Periodontitis Patients Undergoing Hemodialysis
- ClinicalTrials.gov ID
- NCT06726876
- Acronym / sponsor ID
- R626
- Conditions
- Periodontitis, Hemodialysis
- Keywords
- Manuka honey, fibroblast growth factor-21, periodontitis, hemodialysis
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 150 participants (estimated)
- Lead sponsor
- Ain Shams UniversityUniversity, hospital or other
- Study start
- 1 Oct 2024 (actual)
- Primary completion
- 30 Dec 2025 (estimated)
- Study completion
- 30 Dec 2025 (estimated)
- First posted
- 10 Dec 2024 (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.
Chronic Kidney Disease (CKD) has a strong association with chronic periodontitis, an oral disease causing tooth loss linked to inflammation and malnutrition. While periodontitis affects 12.7% of the general population, its prevalence can rise to 39% in certain racial groups, and a dose-response relationship exists with CKD. End Stage Renal Disease (ESRD) patients show a prevalence of periodontitis ranging from 29% to 85.6%. Uremia, immunosuppression, and vitamin D deficiency are suggested factors in the etiology of periodontitis in CKD patients, with uremic toxins potentially altering the oral ecosystem.
Periodontitis involves bacterial biofilm and Gram-negative anaerobes as primary etiological factors. The main treatment goal is to reduce periodontal pathogens and control inflammation, with non-surgical periodontal therapy (NSPT) being the standard. Although various adjuncts like antibiotics and antiseptics are suggested, recent guidelines only recommend certain locally administered agents and systemic antibiotics for specific groups due to increasing bacterial resistance.
Alternative treatments like honey have gained interest, particularly Manuka honey, known for its antibacterial properties against antibiotic-resistant bacteria. This honey's effectiveness is due to its high sugar concentration, low pH, and formation of hydrogen peroxide. Manuka honey's unique component, methylglyoxal (MGO), is a potent bactericide, virucide, and fungicide, linked to its Non-Peroxide Activity (NPA) and Unique Manuka Factor (UMF) rating. MGO also has immunomodulatory effects beneficial for wound healing and tissue regeneration.
Previous studies show Manuka honey as a promising adjunct in NSPT, improving outcomes significantly without adverse effects. Ongoing research aims to evaluate its effects in ESRD patients on hemodialysis, focusing on clinical attachment levels, other periodontal parameters, and FGF 21 levels in gingival crevicular fluid.
Detailed description
Chronic Kidney Disease (CKD) is associated with a high prevalence of chronic periodontitis, an infectious oral disease that causes tooth loss and is linked to inflammation and malnourishment [1]. The frequency of periodontitis is 12.7% in the general population, according to recent epidemiological studies [2], but it can reach as high as 39% in certain racial groups [3, 4], and there is a dose-response relationship with CKD [5]. The prevalence of periodontitis in End Stage Renal Disease (ESRD) has been reported in smaller studies to range from 29 to 85.6% [6, 7, 8]. It has been proposed that uremia and associated immunosuppression, as well as vitamin D deficiency, play a role in the etiology of periodontitis in CKD [5, 9, 10].
Uremic toxins may potentially alter the oral ecosystem (hydrolysis of urea results in alkaline pH) promoting the growth of periodontal pathogens, in a similar manner to the demonstrated uremia-related changes in the gut environment [11, 12]. Studies using microbiological methods of limited scope have shown that ESRD individuals with periodontitis have increased levels of periodontal pathogens as compared to non-CKD controls [13].
Periodontitis is a chronic inflammatory disease affecting the teeth's supporting apparatus. Bacterial biofilm and the associated periodontal pathogenic bacteria, mainly Gram-negative anaerobes, are the main etiological factor of the disease [14].
The main goal of periodontal treatment is to reduce the number of periodontal pathogens and arrest the inflammatory process. The contemporary gold treatment standard is non-surgical periodontal therapy (NSPT), which involves scaling and root planning using manual and machine-driven (sonic or ultrasonic) instruments [15].
Various systemically administered and locally delivered adjuncts to NSPT have been suggested, including systemic and local antibiotics, antiseptics, probiotics, lasers, and photodynamic treatment. However, the latest guidelines on the treatment of periodontitis stage I-III do not support the use of adjuncts. The exception in terms of open recommendations is given for locally administered sustained-release chlorhexidine and antibiotics and the use of systemic antibiotics in specific patient groups [15].
The fact that bacteria are becoming increasingly resistant to antibiotics and antiseptics has shifted the interest of medicine to alternative treatment methods against which bacterial resistance cannot be developed. This approach includes using honey, which is increasingly used in medicine. Since the 1990s, when the first studies appeared on the therapeutic effects of honey, particular interest has been focused on its antibacterial properties against infections and antibiotic-resistant bacteria. This effect is consequential mainly of the high sugar concentration of honey, its low pH value, and the formation of hydrogen peroxide that occurs in the enzymatic breakdown of glucose by the glucose oxidase enzyme [16]. Contemporary research on the effects of honey focuses predominantly on one specific honey type, leading to the medicinal use of Manuka honey due to its antibacterial properties [17]. This is an endemic type of honey produced by bees in Australia and New Zealand from the flowers of the plant Leptospermum scoparium [18].
The concentration of hydrogen peroxide in Manuka honey is lower than in other types of honey [19]. The specific antibacterial activity in Manuka honey is based on methylglyoxal (MGO), a compound proven to be a very efficient bactericide, virucide, and fungicide. Furthermore, Manuka honey is highly effective against antibiotic-resistant bacteria [20].
The antibacterial potency of Manuka honey was found to be related to its Non-Peroxide Activity (NPA), trademarked as Unique Manuka Factor (UMF) rating, a classification system which reflects the equivalent concentration of phenol (%, w/v) required to produce the same antibacterial activity as honey, and it is correlated with the methylglyoxal and total phenols content [21]. In addition to its antimicrobial properties, published literature suggests that MGO also has immunomodulatory effects which may positively impact wound healing and tissue regeneration [22,23].
A previous pilot study indicated a promising potential of Manuka honey as an adjunct in NSPT. Despite the improvement in outcomes appearing modest in absolute terms, it was statistically significant for all follow-up time points, indicating the potential use of Manuka honey as a simple and affordable adjunct to non-surgical periodontal therapy. Furthermore, the product is considered a safe adjunct and no adverse events related to its use were reported during the study period. Encouraging results from this pilot study led to a further randomized clinical study on a larger sample that is currently being performed by our group [24].
Manuka honey oral rinse has not yet been investigated as a possible adjunct to NSPT in ESRD patients on regular hemodialysis. Therefore, this study aims to evaluate the effects of Manuka honey oral rinse on clinical attachment level (CAL) as a primary objective, and other periodontal parameters like (BOP, plaque index), and its effect on the levels of FGF 21 in gingival crevicular fluid as secondary objectives after nonsurgical periodontal treatment in patients with periodontitis.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control Group | Placebo comparator | Drug: Normal saline rinses.Treatment: Normal saline rinse. Protocol: Follow the same protocol as the intervention group but using normal saline rinses instead of Manuka honey. Additional Treatment: Patients will receive scaling and root debridement and locally delivered 0.5 ml non-diluted Thyme honey on sites with PPD ≥ 5 mm. Supplementary Care: Motivation, oral hygiene instructions (proper tooth brushing technique, flossing, interdental brush, mouthwash usage), scaling, polishing, and root debridement with an ultrasonic scaler and Gracey curettes. |
| Intervention Group | Experimental | Dietary Supplement: Manuka honey oral rinse.Treatment: Manuka honey oral rinse. Protocol: Applied as an oral rinse based on the Biswal et al. administration protocol. Patients will have oral rinses (20 ml of Manuka honey diluted in 100 ml of purified water) 3 times per day. Patients will be instructed not to swallow the Manuka honey oral rinse. Additional Treatment: Patients will receive scaling and root debridement and locally delivered 0.5 ml non-diluted Thyme honey on sites with PPD ≥ 5 mm. Supplementary Care: Motivation, oral hygiene instructions (proper tooth brushing technique, flossing, interdental brush, mouthwash usage), scaling, polishing, and root debridement with an ultrasonic scaler and Gracey curettes. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- Both genders, aged above 18 years.
- All patients must be clinically diagnosed of ESRD undergoing hemodialysis.
- All patients must have a periodontal disease.
- Patients must be able to make reliable decision or communications.
Key exclusion criteria (5 listed)
- Smoking, Alcohol.
- Patient with history of any serious illness as malignancy, who undergo kidney transplant.
- Patients with any autoimmune disease.
- Vulnerable groups such as pregnant females, prisoners, mentally and physically handicapped individuals.
- Known hypersensitivity or severe adverse effects to the treatment drugs or to any ingredient of their preparation.
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 |
|---|---|---|
| Manuka honey oral rinse.Name: Manuka Honey Oral Rinse Description: Dosage: Patients will use 20 ml of Manuka honey diluted in 100 ml of purified water. Administration: Oral rinse, performed 3 times per day. Instructions: Patients are instructed to rinse their mouths with the solution for a specified duration and avoid swallowing it. Unique Elements: Active Ingredient: Manuka honey, known for its unique antibacterial properties due to high levels of methylglyoxal (MGO). Mechanism of Action: MGO and Non-Peroxide Activity (NPA) contribute to antibacterial potency, effective against antibiotic-resistant bacteria, and potential immunomodulatory effects that aid wound healing and tissue regeneration. Additional Procedures: Scaling and root debridement, along with the local application of 0.5 ml non-diluted Thyme honey on sites with Probing Pocket Depth (PPD) ≥ 5 mm. Supplementary Care: Patients receive motivation and detailed oral hygiene instructions (proper tooth brushing technique, flossing, use of inte | Dietary supplement | Intervention Group |
| Normal saline rinses.Dosage: Patients will use 20 ml of normal saline. Administration: Oral rinse, performed 3 times per day. Instructions: Patients are instructed to rinse their mouths with the saline solution for a specified duration and avoid swallowing it. Unique Elements: Control Comparison: Provides a placebo comparison to evaluate the efficacy of the Manuka honey intervention. Additional Procedures: Scaling and root debridement, along with the local application of 0.5 ml non-diluted Thyme honey on sites with Probing Pocket Depth (PPD) ≥ 5 mm. | Drug | Control Group |
Primary outcome
Clinical Attachment Level (CAL)
Time frame: Evaluated at baseline, 3 months, and 6 months post-treatment.
Description: Measurement of the attachment level of the periodontal ligament to the tooth surface, indicating the health of periodontal tissues.
6 secondary outcomes
Bleeding on Probing (BOP)
Time frame: Evaluated at baseline, 3 months, and 6 months post-treatment.
Plaque Index
Time frame: Evaluated at baseline, 3 months, and 6 months post-treatment.
Fibroblast Growth Factor 23 (FGF 23) Levels in Gingival Crevicular Fluid (GCF)
Time frame: Evaluated at baseline and at 6 months post-treatment.
Fibroblast Growth Factor 23 (FGF 23) Levels in serum
Time frame: Evaluated at baseline and at 6 months post-treatment.
Oral Health Impact Profile (OHIP-14) scores
Time frame: baseline, and 6 months
Serum C-Reactive Protein (CRP)
Time frame: baseline, 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 31 Dec 2025.
- Derived from this study: PubMed 42556897Abou-Bakr A, Nagi N, Ibrahim M, Alqahtani AS, Hassanein FEA. ADJUNCTIVE MANUKA HONEY ORAL RINSE IN NONSURGICAL PERIODONTAL THERAPY FOR HEMODIALYSIS PATIENTS: A RANDOMIZED CONTROLLED CLINICAL STUDY. J Evid Based Dent Pract. 2026 Sep;26(3):102312. doi: 10.1016/j.jebdp.2026.102312. Epub 2026 May 22.
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Manuka honey oral rinse. and Normal saline rinses. in people with Periodontitis and Hemodialysis, run by Ain Shams University at 1 site in Egypt.
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 4 inclusion and 5 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 31 Dec 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 Egypt. 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.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Clinical Attachment Level (CAL) (time frame: Evaluated at baseline, 3 months, and 6 months post-treatment.). 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 NCT06726876, which also lists 1 linked publication.
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 31 Dec 2025.