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Effect of Piezoelectric Surgery onPostoperative Complications in Third Molar Surgery

E

Ege University

Status

Completed

Conditions

Oral Complication

Treatments

Procedure: conventional surgery
Procedure: piezoelectric surgery

Study type

Interventional

Funder types

Other

Identifiers

NCT06965855
EGE-DHF-MZ-003

Details and patient eligibility

About

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.

Enrollment

60 patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

30 patients in the piezoelectric surgery group
Experimental group
Treatment:
Procedure: piezoelectric surgery
30 patients in the conventional surgery group
Experimental group
Treatment:
Procedure: conventional surgery

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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