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Effect of Piezoelectric Surgery onPostoperative Complications in Third Molar Surgery

NCT06965855 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-05-11

No results posted yet for this study

Summary

The purpose of this study is to compare the effects of piezoelectric surgery on postoperative edema, trismus and other postoperative complications (Wound Healing, Bleeding, Infection, Alveolitis, Paresthesia) with conventional bur method applied in surgical extraction of impacted mandibular third molars.

The main question it aims to answer is:

Is piezoelectric surgery effective on reducing the edema, trismus and other postoperative complications (Wound Healing, Bleeding, Infection, Alveolitis, Paresthesia) in impacted third molar surgery? Postoperative edema measurements are determined at 24 hours, 48 hours, and 7 days using the flexible ruler method. Trismus is determined by measuring the interincisal distance. Statistical analyses are performed to compare the two surgical methods.

Conditions

  • Oral Complication

Interventions

PROCEDURE

conventional surgery

This retrospective clinical study included 30 patients who underwent extraction of impacted lower third molars with conventional surgery

PROCEDURE

piezoelectric surgery

Description: This retrospective clinical study included 30 patients who underwent extraction of impacted lower third molars with piezoelectric surgery

Sponsors & Collaborators

  • Ege University

    lead OTHER

Principal Investigators

  • Mert Zeytinoğlu · Ege University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-01-01
Primary Completion
2012-06-01
Completion
2013-01-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06965855 on ClinicalTrials.gov