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The Effect of Different Flap Closure Techniques on Postoperative Morbidity in Impacted Third Molar Surgery

Study acronym: GMC02
StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated June 9, 2026 (before its estimated August 15, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Start date changed from estimate of Feb 1, 2026 to May 8, 2026
    • Primary completion pushed from May 31, 2026 to Aug 15, 2026
    • Study completion pushed from Jun 30, 2026 to Aug 30, 2026
    v4
  2. Start date: Aug 15, 2025 to Feb 1, 2026
    • Enrollment target: 138 to 148
    • Primary completion date: Dec 15, 2025 to May 31, 2026
    • Study completion date: Dec 15, 2025 to Jun 30, 2026
    v3
  3. Secondary endpoints: details revised at 2 of 2 entries
    • Site details revised
    • Study title shortened, about 4 words
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
1\. ABSTRACT This study is a randomized controlled trial comparing the clinical efficacy and safety of four different flap closure techniques in reducing postoperative morbidity (pain, swelling, trismus, wound healing) and improving patient quality of life (GOHAI) following impacted mandibular third molar extraction. The methods include conventional suturing, sutureless technique, surgical drain, and cyanoacrylate tissue adhesive, which are commonly used in oral surgery practice. The study aims to scientifically evaluate the effects of each method on patients and to determine the most appropriate clinical approach.
Trial Details
NCT Number NCT07198282
Lead Sponsor Recep Tayyip Erdogan University
Conditions
(from sponsor)		 Impacted Mandibular Third Molar, Postoperative Morbidity, Oral Surgery
Enrollment 148 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov