About this trial
This randomized controlled clinical trial aims to evaluate the effectiveness of non-surgical periodontal therapy (NSPT) with and without the adjunctive use of injectable platelet-rich fibrin (I-PRF) in patients with chronic periodontitis. The primary objective is to assess changes in key periodontal parameters including probing depth (PD), clinical attachment level (CAL), bleeding on probing (BOP), and plaque index (PI) over a defined follow-up period. Participants will be randomly assigned to two groups: one receiving standard NSPT alone and the other receiving NSPT combined with subgingival application of I-PRF. The study seeks to determine whether the adjunctive use of I-PRF can enhance periodontal healing and improve clinical outcomes compared to conventional therapy alone.
Eligibility criteria
Qualifiers
None
Disqualifiers
Systemic disease, Smoking, Pregnancy, History of Chemotherapy, Radiotherapy
Trial design
Treatments tested in this trial
- non-surgical periodontal therapy
- non-surgical periodontal therapy + I-PRF
Treatment groups
Sponsors and collaborators
Cairo University
Lead sponsor
Gulf Medical University
Collaborator