Hypertension Clinical Trial
Official title:
Beneficial Effects of Specific Natural Products on Management of Xerostomia: A Randomized Controlled Clinical Trial
NCT number | NCT06217614 |
Other study ID # | 22-018 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 1, 2022 |
Est. completion date | October 1, 2022 |
Verified date | May 2024 |
Source | British University In Egypt |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Xerostomia, the subjective feeling of oral dryness, is a symptom most frequently accompanied by either decreased salivary flow or an altered composition of saliva. Hyposalivation, on the other hand, is the objective measured reduction in salivary flow rate. Xerostomia is a relatively common complaint, particularly among older people, and can lead to major consequences with regard to the quality of their general and oral health and wellbeing. Xerostomia has a variety of possible etiological factors; it is generally classified as having primary and secondary causes. Primary causes comprise conditions that directly affect the salivary glands and induce xerostomia like, Sjogren's syndrome, diabetes mellitus type 1 and 2, thyroid disease, adrenal pathology, renal or hepatic diseases, hepatitis C virus infection, and HIV disease.
Status | Completed |
Enrollment | 28 |
Est. completion date | October 1, 2022 |
Est. primary completion date | September 1, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 19 Years and older |
Eligibility | Inclusion Criteria: - - Both genders, aged above 19 years. - All patients must have complaint of xerostomia. - Objective dry mouth score from (2-5). - Subjective dry mouth score from (1-4). - Patients must be able to make reliable decision or communications. Exclusion Criteria: - - Smoking, Alcohol. - Patient with history of any serious illness as malignancy. - 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. |
Country | Name | City | State |
---|---|---|---|
Egypt | The British University in Egypt | Cairo |
Lead Sponsor | Collaborator |
---|---|
British University In Egypt |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in subjective dry mouth score | subjective dry mouth scores were calculated as the number of asked questions about dry mouth symptoms (0-4), and patients with a score higher than 1 considered having xerostomia so higher scores more than 1 out of 4 indicating xerostomia but lower scores suggesting improvement. | one month | |
Secondary | Changes in objective dry mouth score | Objective dry mouth scores were calculated as the number of observed dry mouth signs (0-5), and patients with a score higher than 2 having xerostomia so higher scores more than 2 out of 5 indicating xerostomia but lower scores suggesting improvement | one month | |
Secondary | Salivary flow rates | Eating and talking were prohibited during the time of collection. Unstimulated whole saliva was collected for 5 min by spitting method. The collection will be timed, so that flow rate (mL/min) could be measure.
increasing in the salivary flow rate of the unstimulated saliva is considered improvment |
one month | |
Secondary | Salivary Nitric oxide levels | Increasing in the salivary nitric oxide levels indicating improvment | one month |
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