CompletedNot Applicable

Ultrasonic Bone Scalpel in BSSO

Turkey (Türkiye)40 participantsStarted 2018-12-15

Plain-language 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.

Who can participate

Age range18 Years – 40 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients are included with older than 18 years old, * normal hemoglobin level, international normalized ratio in the average range, * American Society of Anesthesiologists status of ASA I and II. Exclusion Criteria: * The exclusion criteria are neuropathic disease, * recent use of nonsteroidal anti-inflammatory drugs and opioid derivatives, * having preoperative signs of inflammation in the maxillofacial region, * presence of excessive bleeding in the previous surgery, * and allergy to drugs. All patients have given written informed consent.

What they're measuring

Cutting Time

Timeframe: during procedure

neurosensory disturbance

Timeframe: up to six months

Trial details

NCT IDNCT06273189

SponsorTC Erciyes University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-12-15

View on ClinicalTrials.gov More Maxillofacial Abnormalities trials