Clinical Trial

Effects of Using Miswak in Addition to Oral Hygiene Products in Patients With Gingivitis

Not Yet Recruiting
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Summary
This pilot study aims to evaluate the effects of miswak use on the oral biological environment by comparing biochemical parameters obtained from saliva and dental plaque samples collected from individuals who use miswak and controls. A total of 36 healthy volunteers will be enrolled in the study, including 18 miswak+rutine oral hygiene products users and 18 rutine oral hygiene products. Periodontal clinical parameters will be recorded, and saliva and supragingival dental plaque samples will be collected from all participants. The collected samples will be analysed for biomarkers associated with periodontal inflammation and oxidative stress. Interleukin-1 beta (IL-1β), C-reactive protein (CRP), and oxidative stress levels will be measured using biochemical analysis. The findings of this study are expected to provide preliminary evidence regarding the biological effects of miswak on oral health and contribute to the current understanding of its potential role as an adjunctive oral hygiene tool.
Trial Details
NCT Number NCT07689786
Lead Sponsor Mustafa Kemal University
Conditions Gingivitis; Chronic
Enrollment 36 participants
Start Date 2026-07-04
Primary Completion 2027-07-04 (estimated)
Study Completion 2027-07-04 (estimated)
Updated on ClinicalTrials.gov 2026-07-08