Clinical Trials Directory

Trials / Completed

CompletedNCT07296172

Difficulty, Time & M3 Surgery Outcomes

Surgical Difficulty and Operation Time as Determinants of Outcomes in Mandibular Third Molar Surgery

Status
Completed
Phase
Study type
Observational
Enrollment
150 (actual)
Sponsor
Bahçeşehir University · Academic / Other
Sex
All
Age
15 Years – 60 Years
Healthy volunteers
Not accepted

Summary

This prospective observational cohort study is designed to evaluate early postoperative complications and patient-reported satisfaction following surgical extraction of impacted mandibular third molars under local anesthesia in adult patients. Standardized surgical and postoperative protocols are applied to all participants. The primary objective is to assess overall patient satisfaction on postoperative day 7 using a structured questionnaire. Secondary objectives are to describe the frequency and characteristics of early postoperative pain, swelling, trismus and other complications in the first postoperative week after surgery.

Detailed description

Adult patients requiring surgical removal of an impacted mandibular third molar under local anesthesia will be prospectively enrolled at a single oral and maxillofacial surgery center. All procedures will be performed using a standardized surgical technique and a uniform postoperative medication and care protocol. Clinical examinations and patient-reported outcome measures will be obtained at baseline and at the postoperative day-7 follow-up visit. The study focuses on describing the early postoperative course after third molar surgery and on exploring how early complications relate to overall patient satisfaction with treatment.

Conditions

Timeline

Start date
2017-01-01
Primary completion
2017-05-01
Completion
2017-06-01
First posted
2025-12-22
Last updated
2025-12-22

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT07296172. Inclusion in this directory is not an endorsement.