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RECRUITING
NCT07742826
NA

Comparison of PRF and Corticosteroids in Impacted Third Molar Surgery

Sponsor: Final International University

View on ClinicalTrials.gov

Summary

This prospective, randomized interventional study aims to compare the postoperative effects of standard treatment (control), platelet-rich fibrin (PRF), and PRF combined with corticosteroid treatment in patients undergoing impacted mandibular third molar surgery. A total of 60 participants will be randomly assigned to one of three treatment groups according to the study protocol. Postoperative pain, facial swelling, and trismus will be evaluated on postoperative days 1, 2, 3, and 7. The findings of this study are expected to provide evidence regarding the effectiveness of PRF alone and PRF combined with corticosteroid treatment in reducing postoperative complications following impacted mandibular third molar surgery.

Official title: Comparison of Postoperative Effects of PRF and Corticosteroid Treatments in Impacted Third Molar Surgery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2024-09-03

Completion Date

2026-08

Last Updated

2026-08-03

Healthy Volunteers

Yes

Interventions

BIOLOGICAL

Platelet-rich fibrin (PRF)

Autologous platelet-rich fibrin (PRF) prepared from the participant's venous blood by centrifugation at 3000 rpm for 10 minutes, and then placed into the extraction socket immediately after impacted mandibular third molar surgery.

DRUG

Dexamethasone

Dexamethasone (8 mg/2 mL) administered as a single intramuscular injection immediately after impacted mandibular third molar surgery in addition to platelet-rich fibrin (PRF), according to the study protocol.

DRUG

Amoxicillin/Clavulanic Acid

Amoxicillin/clavulanic acid administered postoperatively according to the study protocol.

DRUG

Paracetamol

Paracetamol 500 mg tablets administered postoperatively for pain control according to the study protocol.

DRUG

Chlorhexidine

Chlorhexidine mouthwash administered postoperatively according to the study protocol.

Locations (1)

Final International University Faculty of Dentistry

Nicosia, Cyprus