Clinical Trial

This a Clinical Trial to Evaluate the Efficacy of I-PRF, Povidone-Iodine and Laser as Adjuncts to Non-surgical Periodontal Treatment in Smokers and Non-Smokers Periodontitis Patients

Recruiting Phase 4
View on ClinicalTrials.gov →
Summary
This study is a randomized, controlled, split-mouth clinical trial designed to evaluate and compare the effectiveness of four different subgingival adjuncts used along side standard Scaling and Root Planning (SRP). This protocol is designed to be a standardized therapeutic model. The subgingival adjuncts are standardized, ensuring that the results are not operator dependent and can be replicated across any dental unit. The primary goal of this study is to evaluate the clinical efficacy of three distinct adjunctive strategies: Biological (I-PRF), Antiseptic : Povidone- iodine , Diode-Laser activation, compared to a Saline Control in the initial treatment of stage 2, 3 and stage 4 of the 2018 AAP/EFP periodontal classification.
Trial Details
NCT Number NCT07707063
Lead Sponsor Military Hospital of Tunis
Conditions Periodontitis, Smokers, Non Smokers, Periodontal Disease
Enrollment 50 participants
Start Date 2026-05-25
Primary Completion 2027-05-18 (estimated)
Study Completion 2027-05-18 (estimated)
Updated on ClinicalTrials.gov 2026-07-16