Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
NCT07198282

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

Led by Recep Tayyip Erdogan University · Updated on 2026-01-12

148

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18-40 years
  • Patients with no systemic diseases (ASA I)
  • Patients with impacted mandibular third molars needing extraction, with bone and/or mucosal retention, in similar positions (Pell & Gregory Class 2, Position B; Winter classification vertical or mesioangular)
Not Eligible

You will not qualify if you...

  • Patients classified as ASA II, III, or IV
  • Known allergy to anesthetic solutions
  • Allergy to acrylate
  • Pregnant or breastfeeding women
  • Individuals who smoke 10 or more cigarettes per day
  • Alcohol users
  • Patients using antiplatelet agents
  • Patients using anticoagulants
  • Patients with coagulation disorders
  • Patients with immunosuppressive diseases or on immunosuppressive therapy
  • Patients with acute pain or local infection at the surgical site

AI-Screening

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Trial Site Locations

Total: 1 location

1

Recep Tayyip Erdoğan University, Faculty of Dentistry, Department of Oral and Maxillofacial Surgery

Rize, Rize Province, Turkey (Türkiye)

Actively Recruiting

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Research Team

A

Alperen Kalyoncu, Assistant Professor

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

4

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