Evaluation of The Periodontal Parameters Following Non-Surgical Periodontal Therapy With and Without Adjunctive Use of Injectable Platelet Rich Fibrin: A Randomized Controlled Clinical Trial

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
AgeUp to 70
SponsorCairo University

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

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Cairo University

Lead sponsor

Gulf Medical University

Collaborator