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Ultrasonic Bone Scalpel in BSSO

NCT06273189 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2024-02-22

No results posted yet for this study

Summary

The conventional saw compared with the piezo surgery in BSSO to evaluate cutting time, surgery duration, amount of bleeding. The purpose of this study was to answers following clinical questions: Is ultrasonic bonescalpel effective osteotomy like conventional bur in BSSO? and 2) Does it reduce operative parameter like bleeding, duration, lingual split pattern? 3) Does it reduce postoperative morbidity after BSSO.

Conditions

  • Maxillofacial Abnormalities

Interventions

DEVICE

Conventional

In conventional group, contralateral side mandibular osteotomies were performed with Lindeman and round bur (Karl Storz, Tuttlingen, Germany)

DEVICE

Bone Scalpel

In ultrasonic device group, osteotomies one side of the mandible were performed unilaterally using an ultrasonic bone scalpel (BoneScalpel; Misonix, Farmingdale, NY) with a serrated standard blade

Sponsors & Collaborators

  • TC Erciyes University

    lead OTHER

Principal Investigators

  • Ahmet Emin Demirbaş, PhD,DDS · Erciyes U

  • Yusuf Nuri Kaba, PhD,DDS · Erciyes U

  • Suheyb Bilge, PhD,DDS · Erciyes U

  • Selin Çelebi, PhD,DDS · Erciyes U

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2018-12-15
Primary Completion
2020-12-15
Completion
2021-12-15

Countries

  • Turkey (Türkiye)

Study Locations

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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 NCT06273189 on ClinicalTrials.gov