MedTrace Logo

Post-Surgical Morbidity and Bone Healing of Impacted Lower Third Molars: Piezosurgery vs. Conventional Instruments

NCT06262841 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2024-02-16

No results posted yet for this study

Summary

The aim of this study is to compare piezosurgery and conventional surgery in impacted third molar surgery and to determine its effect on postoperative outcomes and quality of life.

Conditions

  • Impacted Third Molar Tooth

Interventions

DEVICE

Piezosurgery

Piezosurgery used as an osteotomy device

DEVICE

Conventional burs

Conventional burs used as an osteotomy device

Sponsors & Collaborators

  • Ankara University

    lead OTHER

Principal Investigators

  • Murat K Erdem, PhD, DDS · Ankara University Faculty of Dentistry

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-01
Primary Completion
2023-04-01
Completion
2023-04-01

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

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 NCT06262841 on ClinicalTrials.gov