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Clinical Trial Summary

To evaluate the effectiveness of resveratrol mouthwash as adjunct to NSP treatment of periodontitis


Clinical Trial Description

- Measuring and comparing the efficacy of RV mouth wash in comparison with CHX and placebo mouth wash in improving the clinical periodontal parameters; - Measuring the salivary cytokines (IL-6) before and after 4weeks of the use of RV mouth wash as adjunct to NSP treatment in comparison with other mouthwash by using enzyme-linked immunosorbent assay. - Measuring the salivary RANKL before and after 4weeks of the use of RV mouth wash as adjunct to NSP treatment in comparison with other mouthwash by using enzyme-linked immunosorbent assay. - Correlate the salivary cytokines IL-6 and salivary RANKL with clinical periodontal parameter and with each other. - Evaluate the intervention by using Visual analog scale (VAS)- score-based questionnaire will be filled out by each participant at the end of the trial. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05874882
Study type Interventional
Source University of Baghdad
Contact Hadeel MA [hakram], master
Phone 07703991957
Email hadeel.mazin@codental.uobaghdad.edu.iq
Status Recruiting
Phase Early Phase 1
Start date December 12, 2022
Completion date December 2023

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