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Completed
NCT07748585
Effect of Titanium-Prepared Platelet-Rich Fibrin and Low-Level Laser Therapy on Postoperative Morbidity After Mandibular Third Molar Surgery
Conditions: Impacted Mandibular Third Molar Extraction
Sex: All
Ages: 18 Years – 31 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 60
Sponsor: NEW Cyprus Health and Social Sciences University
Location: Cyprus Health and Social Sciences University, Faculty of Dentistry Güzelyurt Güzelyurt
Summary
This randomized double-blind clinical trial aims to evaluate the effects of titanium-prepared platelet-rich fibrin (T-PRF), low-level laser therapy (LLLT), and their combination on postoperative outcomes following surgical extraction of impacted mandibular third molars. Sixty patients will be randomly allocated to one of four parallel groups: T-PRF, LLLT, T-PRF plus LLLT, or control. The primary outcomes include postoperative pain assessed using a visual analogue scale (VAS), analgesic consumption, postoperative swelling and trismus. The findings may help identify effective approaches for improving postoperative recovery after mandibular third molar surgery.
Eligibility Criteria
Inclusion Criteria:
* Adults requiring surgical extraction of a unilateral vertically impacted mandibular third molar.
* Healthy individuals (ASA I or II).
* Ability to provide written informed consent.
* Willingness to attend all follow-up visits.
Exclusion Criteria:
* Systemic disease affecting wound healing.
* Pregnancy or lactation.
* Active infection or acute pericoronitis.
* Long-term opioid use.
* Smoking and alcohol use.
* Known allergy to study medications.
* Previous radiotherapy to the head and neck region
* Inability to attend follow-up visits.
Source: ClinicalTrials.gov (NCT07748585). StuddyBuddy aggregates publicly available trial information.