Effect of Piezoelectric Surgery onPostoperative Complications in Third Molar Surgery

NCT ID: NCT06965855

Last Updated: 2025-05-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-01-01

Study Completion Date

2013-01-01

Brief Summary

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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.

Detailed Description

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Conditions

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Oral Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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30 patients in the piezoelectric surgery group

Group Type EXPERIMENTAL

piezoelectric surgery

Intervention Type PROCEDURE

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

30 patients in the conventional surgery group

Group Type EXPERIMENTAL

conventional surgery

Intervention Type PROCEDURE

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

Interventions

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conventional surgery

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

Intervention Type PROCEDURE

piezoelectric surgery

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

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with mesioangular, distoangular, vertical or horizontal, fully impacted and fully bone retained impacted lower wisdom teeth
* Patients without any systemic disease
* Patients who have been informed about the duration, purpose and requirements of the study and who have signed the informed consent form voluntarily.

Exclusion Criteria

* Patients with any systemic contraindication, infection in the area of the tooth to be extracted, anamnesis of sensitivity to paracetamol derivatives or aspirin, pregnant or breastfeeding patients, and patients using antibiotics or anti-inflammatory drugs in the last 3 weeks
* In addition, smokers or alcohol addicts were not included in the study.
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ege University

OTHER

Sponsor Role lead

Responsible Party

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Mert Zeytinoğlu

Assoc. Prof. Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mert Zeytinoğlu

Role: PRINCIPAL_INVESTIGATOR

Ege University

Other Identifiers

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EGE-DHF-MZ-003

Identifier Type: -

Identifier Source: org_study_id

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