XerostomiaPhase 4NCT06201923
The Efficacy of Thyme Honey Mouth Rinse on Polypharmacy-induced Xerostomia
A Phase 4 study testing Honey Mouthwash and Normal saline in people with Xerostomia, run by Ain Shams University at 1 site in Egypt.
Trial summary
The study is designed to evaluate the clinical efficacy of thyme honey as a mouth rinse in the management of polypharmacy-induced xerostomia concerning the unstimulated whole salivary flow rate and quality of life of patients along with a biochemical assessment of salivary nitric oxide levels. Read more about this study
- Who is it for?
- Ages 40 to 65 yearsHealthy volunteers can take part
- Conditions the study is for
- Xerostomia
- What is being tested?
- Honey Mouthwash and Normal saline
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 32 participants
- Where
- 1 siteEgypt
- Study dates
- 15 Jan 2024to 2 Dec 2024
- Phase
- Phase 4
- 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 40 to 65 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Both genders, aged between 40 and 65 years old.
- Patients using two or more medications known to cause xerostomia or salivary hypofunction (e.g., anxiolytics, anorexiants, anti-asthmatics, anticholinergics, anti-depressants, anti-emetics, anti-histamines, antihypertensives, anti-parkinsonians, anti-psychotics, antithrombotics, muscle relaxants, anticonvulsants, decongestants, diuretics, NSAIDs, or sedatives). Patients taking previous drugs for 240 days or more before the start of the trial and expected to continue.
- Patients are willing to follow all the instructions and attend all the study-associated visits.
Who cannot join
- Patients who had received radiation therapy to the head and neck region.
- Patients with other systemic diseases known to cause xerostomia (diabetes mellitus, Sjogren's syndrome, rheumatoid arthritis, systemic lupus erythematosus, hepatitis C virus, tuberculosis, or sarcoidosis).
- Patients using any other medication for their dry mouth condition (pilocarpine, cevimeline) 7 days before entering into the study.
- Patients requiring hospitalization for any medical problem during the study.
- Known hypersensitivity to the active ingredient of the product that will be used as assessed by the medical history questionnaire.
- Vulnerable groups such as pregnant females, prisoners, and mentally or physically handicapped individuals.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: The Efficacy of Thyme Honey Mouth Rinse on Polypharmacy-induced Xerostomia (A Randomized Controlled Clinical Trial With a Biochemical Assessment)
The study is designed to evaluate the clinical efficacy of thyme honey as a mouth rinse in the management of polypharmacy-induced xerostomia concerning the unstimulated whole salivary flow rate and quality of life of patients along with a biochemical assessment of salivary nitric oxide levels.
Read the detailed description
Saliva is a vital component in the mouth and the preservation of humans' general health depends on good oral health. Saliva contains primarily water (99.5%), followed by a 0.3% mixture of inorganic salts, enzymes, and proteins. There are many functions of saliva such as lubrication, microbial homeostasis, tooth protection, digestion process, taste, buffering, mineralization, and wound healing. So, when the salivary flow or composition changes due to various causes, these functions will be lost. The normal unstimulated salivary flow rate is about 0.3-0.4 ml/min, whereas the stimulated rate is 1.5-2.0 ml/ min. When there is an objective hyposalivation (< 0.1- 0.2 ml/min unstimulated or < 0.5 - 0.7 ml/min stimulated), patients frequently complain of xerostomia. Xerostomia can be defined as a subjective feeling of oral dryness that might be associated with a real decline in the salivary flow. It can be considered a major problem that greatly affects a person's quality of life due to dysphagia occurrence and taste sensation impairment. The prevalence of xerostomia in the general population ranged from 0.9% to 46%. So, it constitutes a serious health issue requiring attention. The causes of xerostomia can be categorized as systemic or local, depending on their nature. Furthermore, xerostomia is classified as permanent or periodic based on how long the symptoms last. Systemic causes of xerostomia included endocrinological (e.g., diabetes mellitus, autoimmune thyroid diseases), autoimmune (e.g., Sjogren's syndrome, rheumatoid arthritis, systemic lupus erythematosus), infectious (e.g., hepatitis C virus), and granulomatous (e.g., tuberculosis and sarcoidosis) diseases, while Local factors of xerostomia comprised multiple medications (polypharmacy), radical radiotherapy for the treatment of head and neck malignancies, and lifestyle factors, such as alcohol, tobacco, and caffeine consumption. Recently, it was also documented that 45.9% of patients with confirmed SARS-CoV-2 infection experienced xerostomia, with a considerable majority (76.5%) of them noting that it was their first time experiencing xerostomia. Polypharmacy is thought to be the most common cause of xerostomia. Several definitions of polypharmacy were reported in the literature. There was a wide range of numerical-only definitions of polypharmacy, ranging from two or more medications to 11 or more medications, Also the numerical definitions of polypharmacy incorporating duration of therapy ranged from the use of two or more medications for more than 240 days (long-term use) to five to nine medications used for 90 days or more, While descriptive definitions explained co-prescribing multiple medications and simultaneous and long-term use of different drugs by the same individual. More than 400 drugs have an impact on the function of the salivary glands and promote the development of xerostomia. Drugs that frequently contribute to xerostomia include antiparkinsonian pharmaceuticals, antipsychotics, antidepressants, anticholinergic, antihistamines, tranquilizers, oral hypoglycemics, diuretics, opioids, cytotoxic agents, and antihypertensive medications. The precise processes by which some drugs produce xerostomia aren't yet understood.
Various treatment modalities can be used to treat xerostomia and salivary hypofunction depending on the underlying cause of the condition, which are classified into systemic and topical agents. The FDA has approved systemic sialogogues, namely pilocarpine, and cevimeline, as a treatment modality. Cevimeline and the other medications are parasympathomimetics and act on muscarinic receptors. Despite their powerful effect, severe highly prevalent side effects are caused after their regular administration including vasodilatation, emesis, excessive sweating, hypotension, bronchoconstriction, increased urinary frequency, bradycardia, and vision problems. Topical and local medications for xerostomia continue to be a more appealing and secure therapy choice. These include sugar-free chewing gums, salivary stimulants, and substitutes. salivary substitutes make an effort to resemble natural saliva and act as oral lubricants without changing the salivary flow rate, and due to their viscosity, they are not commonly used and not accepted by most patients. These substitutes are mainly utilized when completely damaged salivary glands. Topical salivary stimulants are the most popular and widely tolerated among patients mainly used when there is residual functional salivary tissue. These topical stimulants can be divided into acid or mechanically-driven. Mechanical salivary stimulation occurs through the utilization of sugar-free chewing gums which aim to stimulate the major salivary glands to increase the salivary flow. While acid-driven stimulation occurs through acidification of the oral cavity with malic acid, and citric acid to increase the salivary flow rate. One of the topical salivary stimulants that have been recently studied is the thyme honey mouth rinse. Thyme honey is used for xerostomia under the assumption that it has saliva-stimulating effects as it consists of various organic acids such as ascorbic acid, citric acid, and malic acid which are used as saliva stimulators. Previous research has demonstrated that organic acids stimulate the chemoreceptors in the oral cavity, increasing the flow of saliva. Later, thyme honey has proven its efficacy in preventing radiation-induced salivary gland destruction and xerostomia. Thyme honey has antibacterial, antiviral, antifungal, anti-inflammatory, antioxidant, and anticarcinogenic properties. It has been used to treat burns, surgical wounds, and oral infections due to its antibacterial and analgesic properties and ability to promote epithelialization. The majority of honey varieties produce hydrogen peroxide when diluted due to the activation of the enzyme glucose oxidase, which oxidizes glucose to gluconic acid and hydrogen peroxide. The main component of honey's antibacterial activity is hydrogen peroxide as well as the presence of phytochemicals and its acidic environment with a pH ranging from 3.2 to 4.5.
Nitric oxide in the saliva is produced by the nerve ending in the salivary gland's endothelium and macrophages in response to the oral bacteria. Nitric oxide levels rise and oxidative stress occurs as a result of phagocyte induction. So, High levels of nitrate and nitrite (the stable end products of nitric oxide) in typical saliva help to locally produce nitrogen intermediates with possible antibacterial capabilities, enhanced mucosal blood flow, and improved oral mucus formation. The salivary NO level in patients with xerostomia is significantly lower than in those without xerostomia. So, salivary nitric oxide level could be considered a predictor of xerostomia.
- Clinical Assessment: all patients are evaluated at baseline, 2 and 4 weeks after intervention through
- Measurement of Unstimulated Salivary Flow Rate (UFR): by spitting method for assessment of salivary gland hypofunction. Measurements are expressed in millimeters per minute (ml/min). If the unstimulated flow rate is less than 0.2 mL/min. it will be considered to represent salivary gland hypofunction and this patient will be included in the study.
- Measurement of subjective symptoms of oral dryness: by using a questionnaire consisting of four questions that assess the severity of dry mouth. patients will answer these questions with (yes or no). positive response to any question indicates a reduced unstimulated salivary flow rate and this patient will be included in the study. Q1: Does it seem like there isn't enough saliva in your mouth? Q2: Do you ever have trouble swallowing? Q3: Does eating a meal cause your mouth to feel dry? Q4: Do you drink liquids to make it easier to swallow dry food?
- Measurement of objective signs of oral dryness: by using a clinical oral dryness score (CODS) consisting of a 10-point scale, each point representing a feature of dryness in the mouth. The clinician scores the features observed in the patient's mouth from 0-10. Patients with a score less than 2 will be excluded.
- The buccal mucosa becomes stuck with the mirror. 2. The tongue adheres to the mirror. 3. Saliva with foam. 4. There isn't any saliva collecting on the mouth's floor. 5. The papillae of the tongue have disappeared. 6. Modified or smooth gingival structure. 7. The mucosa of the mouth, particularly the palate, appears glassy. 8. Lobular or fissured tongue. 9. Cervical caries that have just been repaired within the past six months (more than two teeth). 10. Debris on the palate (excluding under dentures).
All patients are also evaluated at baseline and after one month from intervention through the following:
- Xerostomia-related quality of life questionnaire: includes 15 questions regarding how dry mouth affects a person's quality of life. The questions are:
- Is the type or quantity of food you can eat restricted by your mouth dryness? 2. Does having a dry mouth make you uncomfortable? 3. Does your oral dryness make you anxious or concerned a lot? 4. Do you avoid social situations because of dry mouth? 5. Is it unsettling to eat in front of others when your mouth is dry? 6. When speaking in front of other people, does your dry mouth make you feel uneasy? 7. Does your oral dryness make you nervous? 8. Are you worried about how your teeth and mouth seem because of your mouth dryness? 9. Do you find it difficult to enjoy life because of your dry mouth? 10. Does having a dry mouth affect your everyday activities? 11. Does your mouth dryness affect the intimacy with your relationships? 12. Does dry mouth affect how well you can taste food? 13. Does having a dry mouth lessen your overall enjoyment of life? 14. Does your mouth dryness interfere with every part of your life? 15. How would you feel if you were forced to live the remainder of your days with a dry mouth the way it is right now? The questionnaire will be translated verbally, and answers will be collected orally from the patients and documented by an investigator not involved in assigning the intervention to patients.
- Biochemical Assessment:
> Measurement of salivary nitric oxide (NO) level: measured at baseline and after one month in the Lab.
Statistical Methods:
All the data will be collected and analyzed statistically. Categorical data will be represented as frequency (n) and percentage (%) and will be analyzed using the chi-square test. Numerical data will be explored for normality by checking the data distribution, calculating the mean and median values, and using Kolmogorov-Smirnov and Shapiro-Wilk tests. If the data was found to be normally distributed, it will be presented as mean and standard deviation values and an independent t-test will be used for the analysis. If the assumption of normality is found to be violated; the data will be presented as median and range values and will be analyzed using the Mann-Whitney U test. The significance level will be set at p ≤0.05 for all tests. Statistical analysis will be performed with IBM® SPSS® Statistics Version 26 for Windows.
- Conditions
- Xerostomia
- Being tested
- Honey Mouthwash, Normal saline
- Medical subject headings
- Xerostomia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Honey MouthwashDrug
Also called thyme honey mouth rinse
0.2% thyme honey mouth rinse
Normal salineDrug
Also called saline mouth rinse
0.9% sodium chloride
| Study group | Role | What they receive |
|---|---|---|
| Group I (Thyme H) | Experimental | 0.2% thyme honey mouth rinse (20 ml of thyme honey diluted in 100 ml of purified water) 3 times per day. Receives: Drug: Honey Mouthwash |
| Group II (Saline G) | Placebo comparator | normal saline oral rinse Receives: Drug: Normal saline |
What is being measured
The primary outcome is the main question the study is designed to answer.
Evaluate the clinical efficacy of 0.2% thyme honey mouth rinse on salivary flow rate of patients having polypharmacy-induced xerostomia
To eliminate any circadian changes, the unstimulated salivary flow rate will be measured for all patients between 9:00 to 11:00 a.m. Before saliva collection, participants are requested to wait at least two hours without eating, drinking, or brushing their teeth. Then, after swallowing all the saliva present in their mouth, unstimulated whole saliva will be collected by spitting method every 60s for 5 min in a sterile tube. The tubes are kept in a refrigerator (-20 centigrade) before sending them to the laboratory to prevent changing the composition of the saliva.
Measured: one month
Secondary outcomes (1)
Evaluate the clinical effect of thyme honey mouth rinse on the quality of life of the patients as well as its biochemical effect on the level of salivary nitric oxide
Xerostomia-related quality of life questionnaire which includes 15 questions will be used.
salivary nitric oxide level will be assessed by Nitric Oxide Assay Kit (Colorimetric) based on the Griess reaction.
Measured: one month
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Jan 2024
- Study start15 Jan 2024
- Primary completion2 Nov 2024
- Study completion2 Dec 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (15)Papers the sponsor has linked to this study.
- Other trials for XerostomiaStudies 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- 0.2% thyme honey mouth rinse as intervention
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 32 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ain Shams University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Neven Nabil Tadry Banoud, Ain Shams University
- Investigators
- Suzan S. Ibrahim, Prof., Study director, Professor of Oral Medicine, Periodontology, Faculty of Dentistry, Ain Shams UniversityOla M. Ezzatt Hassanein, Ass. Prof., Study director, Associate Professor of Oral Medicine, Periodontology, Faculty of Dentistry, Ain Shams University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06201923
- Sponsor's protocol ID
- Thyme Honey Mouth Rinse
- Status last verified
- Jan 2025
- First submitted
- 1 Jan 2024
- Last updated
- 29 Apr 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Publications
Humphrey SP, Williamson RT. A review of saliva: normal composition, flow, and function. J Prosthet Dent. 2001 Feb;85(2):162-9. doi: 10.1067/mpr.2001.113778.
PubMed 11208206Cassolato SF, Turnbull RS. Xerostomia: clinical aspects and treatment. Gerodontology. 2003 Dec;20(2):64-77. doi: 10.1111/j.1741-2358.2003.00064.x.
PubMed 14697016Pedersen AM, Bardow A, Jensen SB, Nauntofte B. Saliva and gastrointestinal functions of taste, mastication, swallowing and digestion. Oral Dis. 2002 May;8(3):117-29. doi: 10.1034/j.1601-0825.2002.02851.x.
PubMed 12108756Napenas JJ, Brennan MT, Fox PC. Diagnosis and treatment of xerostomia (dry mouth). Odontology. 2009 Jul;97(2):76-83. doi: 10.1007/s10266-008-0099-7. Epub 2009 Jul 29.
PubMed 19639449Masnoon N, Shakib S, Kalisch-Ellett L, Caughey GE. What is polypharmacy? A systematic review of definitions. BMC Geriatr. 2017 Oct 10;17(1):230. doi: 10.1186/s12877-017-0621-2.
PubMed 29017448Barbe AG. Medication-Induced Xerostomia and Hyposalivation in the Elderly: Culprits, Complications, and Management. Drugs Aging. 2018 Oct;35(10):877-885. doi: 10.1007/s40266-018-0588-5.
PubMed 30187289Charalambous A, Lambrinou E, Katodritis N, Vomvas D, Raftopoulos V, Georgiou M, Paikousis L, Charalambous M. The effectiveness of thyme honey for the management of treatment-induced xerostomia in head and neck cancer patients: A feasibility randomized control trial. Eur J Oncol Nurs. 2017 Apr;27:1-8. doi: 10.1016/j.ejon.2017.01.001. Epub 2017 Jan 16.
PubMed 28279391Charalambous M, Raftopoulos V, Paikousis L, Katodritis N, Lambrinou E, Vomvas D, Georgiou M, Charalambous A. The effect of the use of thyme honey in minimizing radiation - induced oral mucositis in head and neck cancer patients: A randomized controlled trial. Eur J Oncol Nurs. 2018 Jun;34:89-97. doi: 10.1016/j.ejon.2018.04.003. Epub 2018 Apr 30.
PubMed 29784145Biswal BM, Zakaria A, Ahmad NM. Topical application of honey in the management of radiation mucositis: a preliminary study. Support Care Cancer. 2003 Apr;11(4):242-8. doi: 10.1007/s00520-003-0443-y. Epub 2003 Feb 19.
PubMed 12673463Osailan SM, Pramanik R, Shirlaw P, Proctor GB, Challacombe SJ. Clinical assessment of oral dryness: development of a scoring system related to salivary flow and mucosal wetness. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Nov;114(5):597-603. doi: 10.1016/j.oooo.2012.05.009. Epub 2012 Sep 7.
PubMed 22959491Ship JA, McCutcheon JA, Spivakovsky S, Kerr AR. Safety and effectiveness of topical dry mouth products containing olive oil, betaine, and xylitol in reducing xerostomia for polypharmacy-induced dry mouth. J Oral Rehabil. 2007 Oct;34(10):724-32. doi: 10.1111/j.1365-2842.2006.01718.x.
PubMed 17824884Carpenter GH. The secretion, components, and properties of saliva. Annu Rev Food Sci Technol. 2013;4:267-76. doi: 10.1146/annurev-food-030212-182700.
PubMed 23464573Afsaneh Abadi P, Koopaie M, Montazeri R. Comparison of salivary nitric oxide and oral health in diabetic patients with and without xerostomia. Diabetes Metab Syndr. 2020 Jan-Feb;14(1):11-15. doi: 10.1016/j.dsx.2019.11.014. Epub 2019 Nov 25.
PubMed 31809967Jockel-Schneider Y, Schlagenhauf U, Stolzel P, Gossner S, Carle R, Ehmke B, Prior K, Hagenfeld D. Nitrate-rich diet alters the composition of the oral microbiota in periodontal recall patients. J Periodontol. 2021 Nov;92(11):1536-1545. doi: 10.1002/JPER.20-0778. Epub 2021 Apr 6.
PubMed 33742692Ibrahim SS, Tadry NN, Ezzatt OM, Hussein RR. The efficacy of thyme honey mouth rinse on polypharmacy-induced xerostomia: A randomized controlled clinical trial with a biochemical assessment. J Stomatol Oral Maxillofac Surg. 2026 Feb;127(1):102641. doi: 10.1016/j.jormas.2025.102641. Epub 2025 Nov 4.
PubMed 41192795
Study at a glance
From the registry record, last updated by the sponsor on 29 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Efficacy of Thyme Honey Mouth Rinse on Polypharmacy-induced Xerostomia (A Randomized Controlled Clinical Trial With a Biochemical Assessment)
- ClinicalTrials.gov ID
- NCT06201923
- Acronym / sponsor ID
- Thyme Honey Mouth Rinse
- Conditions
- Xerostomia
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 32 participants (actual)
- Lead sponsor
- Ain Shams UniversityUniversity, hospital or other
- Study start
- 15 Jan 2024 (actual)
- Primary completion
- 2 Nov 2024 (actual)
- Study completion
- 2 Dec 2024 (actual)
- First posted
- 11 Jan 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.
The study is designed to evaluate the clinical efficacy of thyme honey as a mouth rinse in the management of polypharmacy-induced xerostomia concerning the unstimulated whole salivary flow rate and quality of life of patients along with a biochemical assessment of salivary nitric oxide levels.
Detailed description
Saliva is a vital component in the mouth and the preservation of humans' general health depends on good oral health. Saliva contains primarily water (99.5%), followed by a 0.3% mixture of inorganic salts, enzymes, and proteins. There are many functions of saliva such as lubrication, microbial homeostasis, tooth protection, digestion process, taste, buffering, mineralization, and wound healing. So, when the salivary flow or composition changes due to various causes, these functions will be lost. The normal unstimulated salivary flow rate is about 0.3-0.4 ml/min, whereas the stimulated rate is 1.5-2.0 ml/ min. When there is an objective hyposalivation (< 0.1- 0.2 ml/min unstimulated or < 0.5 - 0.7 ml/min stimulated), patients frequently complain of xerostomia. Xerostomia can be defined as a subjective feeling of oral dryness that might be associated with a real decline in the salivary flow. It can be considered a major problem that greatly affects a person's quality of life due to dysphagia occurrence and taste sensation impairment. The prevalence of xerostomia in the general population ranged from 0.9% to 46%. So, it constitutes a serious health issue requiring attention. The causes of xerostomia can be categorized as systemic or local, depending on their nature. Furthermore, xerostomia is classified as permanent or periodic based on how long the symptoms last. Systemic causes of xerostomia included endocrinological (e.g., diabetes mellitus, autoimmune thyroid diseases), autoimmune (e.g., Sjogren's syndrome, rheumatoid arthritis, systemic lupus erythematosus), infectious (e.g., hepatitis C virus), and granulomatous (e.g., tuberculosis and sarcoidosis) diseases, while Local factors of xerostomia comprised multiple medications (polypharmacy), radical radiotherapy for the treatment of head and neck malignancies, and lifestyle factors, such as alcohol, tobacco, and caffeine consumption. Recently, it was also documented that 45.9% of patients with confirmed SARS-CoV-2 infection experienced xerostomia, with a considerable majority (76.5%) of them noting that it was their first time experiencing xerostomia. Polypharmacy is thought to be the most common cause of xerostomia. Several definitions of polypharmacy were reported in the literature. There was a wide range of numerical-only definitions of polypharmacy, ranging from two or more medications to 11 or more medications, Also the numerical definitions of polypharmacy incorporating duration of therapy ranged from the use of two or more medications for more than 240 days (long-term use) to five to nine medications used for 90 days or more, While descriptive definitions explained co-prescribing multiple medications and simultaneous and long-term use of different drugs by the same individual. More than 400 drugs have an impact on the function of the salivary glands and promote the development of xerostomia. Drugs that frequently contribute to xerostomia include antiparkinsonian pharmaceuticals, antipsychotics, antidepressants, anticholinergic, antihistamines, tranquilizers, oral hypoglycemics, diuretics, opioids, cytotoxic agents, and antihypertensive medications. The precise processes by which some drugs produce xerostomia aren't yet understood.
Various treatment modalities can be used to treat xerostomia and salivary hypofunction depending on the underlying cause of the condition, which are classified into systemic and topical agents. The FDA has approved systemic sialogogues, namely pilocarpine, and cevimeline, as a treatment modality. Cevimeline and the other medications are parasympathomimetics and act on muscarinic receptors. Despite their powerful effect, severe highly prevalent side effects are caused after their regular administration including vasodilatation, emesis, excessive sweating, hypotension, bronchoconstriction, increased urinary frequency, bradycardia, and vision problems. Topical and local medications for xerostomia continue to be a more appealing and secure therapy choice. These include sugar-free chewing gums, salivary stimulants, and substitutes. salivary substitutes make an effort to resemble natural saliva and act as oral lubricants without changing the salivary flow rate, and due to their viscosity, they are not commonly used and not accepted by most patients. These substitutes are mainly utilized when completely damaged salivary glands. Topical salivary stimulants are the most popular and widely tolerated among patients mainly used when there is residual functional salivary tissue. These topical stimulants can be divided into acid or mechanically-driven. Mechanical salivary stimulation occurs through the utilization of sugar-free chewing gums which aim to stimulate the major salivary glands to increase the salivary flow. While acid-driven stimulation occurs through acidification of the oral cavity with malic acid, and citric acid to increase the salivary flow rate. One of the topical salivary stimulants that have been recently studied is the thyme honey mouth rinse. Thyme honey is used for xerostomia under the assumption that it has saliva-stimulating effects as it consists of various organic acids such as ascorbic acid, citric acid, and malic acid which are used as saliva stimulators. Previous research has demonstrated that organic acids stimulate the chemoreceptors in the oral cavity, increasing the flow of saliva. Later, thyme honey has proven its efficacy in preventing radiation-induced salivary gland destruction and xerostomia. Thyme honey has antibacterial, antiviral, antifungal, anti-inflammatory, antioxidant, and anticarcinogenic properties. It has been used to treat burns, surgical wounds, and oral infections due to its antibacterial and analgesic properties and ability to promote epithelialization. The majority of honey varieties produce hydrogen peroxide when diluted due to the activation of the enzyme glucose oxidase, which oxidizes glucose to gluconic acid and hydrogen peroxide. The main component of honey's antibacterial activity is hydrogen peroxide as well as the presence of phytochemicals and its acidic environment with a pH ranging from 3.2 to 4.5.
Nitric oxide in the saliva is produced by the nerve ending in the salivary gland's endothelium and macrophages in response to the oral bacteria. Nitric oxide levels rise and oxidative stress occurs as a result of phagocyte induction. So, High levels of nitrate and nitrite (the stable end products of nitric oxide) in typical saliva help to locally produce nitrogen intermediates with possible antibacterial capabilities, enhanced mucosal blood flow, and improved oral mucus formation. The salivary NO level in patients with xerostomia is significantly lower than in those without xerostomia. So, salivary nitric oxide level could be considered a predictor of xerostomia.
- Clinical Assessment: all patients are evaluated at baseline, 2 and 4 weeks after intervention through
- Measurement of Unstimulated Salivary Flow Rate (UFR): by spitting method for assessment of salivary gland hypofunction. Measurements are expressed in millimeters per minute (ml/min). If the unstimulated flow rate is less than 0.2 mL/min. it will be considered to represent salivary gland hypofunction and this patient will be included in the study.
- Measurement of subjective symptoms of oral dryness: by using a questionnaire consisting of four questions that assess the severity of dry mouth. patients will answer these questions with (yes or no). positive response to any question indicates a reduced unstimulated salivary flow rate and this patient will be included in the study. Q1: Does it seem like there isn't enough saliva in your mouth? Q2: Do you ever have trouble swallowing? Q3: Does eating a meal cause your mouth to feel dry? Q4: Do you drink liquids to make it easier to swallow dry food?
- Measurement of objective signs of oral dryness: by using a clinical oral dryness score (CODS) consisting of a 10-point scale, each point representing a feature of dryness in the mouth. The clinician scores the features observed in the patient's mouth from 0-10. Patients with a score less than 2 will be excluded.
- The buccal mucosa becomes stuck with the mirror. 2. The tongue adheres to the mirror. 3. Saliva with foam. 4. There isn't any saliva collecting on the mouth's floor. 5. The papillae of the tongue have disappeared. 6. Modified or smooth gingival structure. 7. The mucosa of the mouth, particularly the palate, appears glassy. 8. Lobular or fissured tongue. 9. Cervical caries that have just been repaired within the past six months (more than two teeth). 10. Debris on the palate (excluding under dentures).
All patients are also evaluated at baseline and after one month from intervention through the following:
- Xerostomia-related quality of life questionnaire: includes 15 questions regarding how dry mouth affects a person's quality of life. The questions are:
- Is the type or quantity of food you can eat restricted by your mouth dryness? 2. Does having a dry mouth make you uncomfortable? 3. Does your oral dryness make you anxious or concerned a lot? 4. Do you avoid social situations because of dry mouth? 5. Is it unsettling to eat in front of others when your mouth is dry? 6. When speaking in front of other people, does your dry mouth make you feel uneasy? 7. Does your oral dryness make you nervous? 8. Are you worried about how your teeth and mouth seem because of your mouth dryness? 9. Do you find it difficult to enjoy life because of your dry mouth? 10. Does having a dry mouth affect your everyday activities? 11. Does your mouth dryness affect the intimacy with your relationships? 12. Does dry mouth affect how well you can taste food? 13. Does having a dry mouth lessen your overall enjoyment of life? 14. Does your mouth dryness interfere with every part of your life? 15. How would you feel if you were forced to live the remainder of your days with a dry mouth the way it is right now? The questionnaire will be translated verbally, and answers will be collected orally from the patients and documented by an investigator not involved in assigning the intervention to patients.
- Biochemical Assessment:
> Measurement of salivary nitric oxide (NO) level: measured at baseline and after one month in the Lab.
Statistical Methods:
All the data will be collected and analyzed statistically. Categorical data will be represented as frequency (n) and percentage (%) and will be analyzed using the chi-square test. Numerical data will be explored for normality by checking the data distribution, calculating the mean and median values, and using Kolmogorov-Smirnov and Shapiro-Wilk tests. If the data was found to be normally distributed, it will be presented as mean and standard deviation values and an independent t-test will be used for the analysis. If the assumption of normality is found to be violated; the data will be presented as median and range values and will be analyzed using the Mann-Whitney U test. The significance level will be set at p ≤0.05 for all tests. Statistical analysis will be performed with IBM® SPSS® Statistics Version 26 for Windows.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, care provider)
- Number of arms
- 2
- Model description
- 0.2% thyme honey mouth rinse as intervention
| Arm | Type | Receives |
|---|---|---|
| Group I (Thyme H) | Experimental | Drug: Honey Mouthwash0.2% thyme honey mouth rinse (20 ml of thyme honey diluted in 100 ml of purified water) 3 times per day. |
| Group II (Saline G) | Placebo comparator | Drug: Normal salinenormal saline oral rinse |
Who may qualify
- Ages
- 40 to 65 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- Both genders, aged between 40 and 65 years old.
- Patients using two or more medications known to cause xerostomia or salivary hypofunction (e.g., anxiolytics, anorexiants, anti-asthmatics, anticholinergics, anti-depressants, anti-emetics, anti-histamines, antihypertensives, anti-parkinsonians, anti-psychotics, antithrombotics, muscle relaxants, anticonvulsants, decongestants, diuretics, NSAIDs, or sedatives). Patients taking previous drugs for 240 days or more before the start of the trial and expected to continue.
- Patients are willing to follow all the instructions and attend all the study-associated visits.
Key exclusion criteria (6 listed)
- Patients who had received radiation therapy to the head and neck region.
- Patients with other systemic diseases known to cause xerostomia (diabetes mellitus, Sjogren's syndrome, rheumatoid arthritis, systemic lupus erythematosus, hepatitis C virus, tuberculosis, or sarcoidosis).
- Patients using any other medication for their dry mouth condition (pilocarpine, cevimeline) 7 days before entering into the study.
- Patients requiring hospitalization for any medical problem during the study.
- Known hypersensitivity to the active ingredient of the product that will be used as assessed by the medical history questionnaire.
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 |
|---|---|---|
| Honey MouthwashAlso: thyme honey mouth rinse0.2% thyme honey mouth rinse | Drug | Group I (Thyme H) |
| Normal salineAlso: saline mouth rinse0.9% sodium chloride | Drug | Group II (Saline G) |
Primary outcome
Evaluate the clinical efficacy of 0.2% thyme honey mouth rinse on salivary flow rate of patients having polypharmacy-induced xerostomia
Time frame: one month
To eliminate any circadian changes, the unstimulated salivary flow rate will be measured for all patients between 9:00 to 11:00 a.m. Before saliva collection, participants are requested to wait at least two hours without eating, drinking, or brushing their teeth. Then, after swallowing all the saliva present in their mouth, unstimulated whole saliva will be collected by spitting method every 60s for 5 min in a sterile tube. The tubes are kept in a refrigerator (-20 centigrade) before sending them to the laboratory to prevent changing the composition of the saliva.
1 secondary outcome
Evaluate the clinical effect of thyme honey mouth rinse on the quality of life of the patients as well as its biochemical effect on the level of salivary nitric oxide
Time frame: one month
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Apr 2025.
- Results publication: PubMed 11208206Humphrey SP, Williamson RT. A review of saliva: normal composition, flow, and function. J Prosthet Dent. 2001 Feb;85(2):162-9. doi: 10.1067/mpr.2001.113778.
- Results publication: PubMed 14697016Cassolato SF, Turnbull RS. Xerostomia: clinical aspects and treatment. Gerodontology. 2003 Dec;20(2):64-77. doi: 10.1111/j.1741-2358.2003.00064.x.
- Results publication: PubMed 12108756Pedersen AM, Bardow A, Jensen SB, Nauntofte B. Saliva and gastrointestinal functions of taste, mastication, swallowing and digestion. Oral Dis. 2002 May;8(3):117-29. doi: 10.1034/j.1601-0825.2002.02851.x.
- Results publication: PubMed 19639449Napenas JJ, Brennan MT, Fox PC. Diagnosis and treatment of xerostomia (dry mouth). Odontology. 2009 Jul;97(2):76-83. doi: 10.1007/s10266-008-0099-7. Epub 2009 Jul 29.
- Results publication: PubMed 29017448Masnoon N, Shakib S, Kalisch-Ellett L, Caughey GE. What is polypharmacy? A systematic review of definitions. BMC Geriatr. 2017 Oct 10;17(1):230. doi: 10.1186/s12877-017-0621-2.
- Results publication: PubMed 30187289Barbe AG. Medication-Induced Xerostomia and Hyposalivation in the Elderly: Culprits, Complications, and Management. Drugs Aging. 2018 Oct;35(10):877-885. doi: 10.1007/s40266-018-0588-5.
- Results publication: PubMed 28279391Charalambous A, Lambrinou E, Katodritis N, Vomvas D, Raftopoulos V, Georgiou M, Paikousis L, Charalambous M. The effectiveness of thyme honey for the management of treatment-induced xerostomia in head and neck cancer patients: A feasibility randomized control trial. Eur J Oncol Nurs. 2017 Apr;27:1-8. doi: 10.1016/j.ejon.2017.01.001. Epub 2017 Jan 16.
- Results publication: PubMed 29784145Charalambous M, Raftopoulos V, Paikousis L, Katodritis N, Lambrinou E, Vomvas D, Georgiou M, Charalambous A. The effect of the use of thyme honey in minimizing radiation - induced oral mucositis in head and neck cancer patients: A randomized controlled trial. Eur J Oncol Nurs. 2018 Jun;34:89-97. doi: 10.1016/j.ejon.2018.04.003. Epub 2018 Apr 30.
- Results publication: PubMed 12673463Biswal BM, Zakaria A, Ahmad NM. Topical application of honey in the management of radiation mucositis: a preliminary study. Support Care Cancer. 2003 Apr;11(4):242-8. doi: 10.1007/s00520-003-0443-y. Epub 2003 Feb 19.
- Results publication: PubMed 22959491Osailan SM, Pramanik R, Shirlaw P, Proctor GB, Challacombe SJ. Clinical assessment of oral dryness: development of a scoring system related to salivary flow and mucosal wetness. Oral Surg Oral Med Oral Pathol Oral Radiol. 2012 Nov;114(5):597-603. doi: 10.1016/j.oooo.2012.05.009. Epub 2012 Sep 7.
- Results publication: PubMed 17824884Ship JA, McCutcheon JA, Spivakovsky S, Kerr AR. Safety and effectiveness of topical dry mouth products containing olive oil, betaine, and xylitol in reducing xerostomia for polypharmacy-induced dry mouth. J Oral Rehabil. 2007 Oct;34(10):724-32. doi: 10.1111/j.1365-2842.2006.01718.x.
- Results publication: PubMed 23464573Carpenter GH. The secretion, components, and properties of saliva. Annu Rev Food Sci Technol. 2013;4:267-76. doi: 10.1146/annurev-food-030212-182700.
- The identification of inhibine, the antibacterial factor in honey, as hydrogen peroxide and its origin in a honey glucose-oxidase systemLink provided by the sponsor.
- Measuring salivary flow: Challenges and opportunitiesLink provided by the sponsor.
- Subjective reports of xerostomia and objective measures of salivary gland performanceLink provided by the sponsor.
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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. This study is not recruiting at the moment.
Suzan S. Ibrahim, Prof. study director
Professor of Oral Medicine, Periodontology, Faculty of Dentistry, Ain Shams University
Ola M. Ezzatt Hassanein, Ass. Prof. study director
Associate Professor of Oral Medicine, Periodontology, Faculty of Dentistry, Ain Shams University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Honey Mouthwash and Normal saline in people with Xerostomia, 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 3 inclusion and 6 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 29 Apr 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
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?
Evaluate the clinical efficacy of 0.2% thyme honey mouth rinse on salivary flow rate of patients having polypharmacy-induced xerostomia (time frame: one month). 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 NCT06201923, which also lists 15 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 29 Apr 2025.