Clinical Trial

Pre-Extubation Bupivacaine for Pain Control After Orthognathic Surgery

Completed
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Summary
This study aims to evaluate whether injecting a long-acting local anesthetic (bupivacaine) at surgical sites before awakening from anesthesia can reduce pain and the need for opioid medications after orthognathic surgery. Orthognathic surgery is a major procedure that can cause significant postoperative pain, often requiring opioid analgesics, which may lead to side effects such as nausea, vomiting, and drowsiness. In this randomized clinical study, patients undergoing jaw surgery received either standard care or additional bupivacaine infiltration before extubation. Pain levels and opioid consumption were measured during the first 48 hours after surgery. We hypothesized that pre-extubation bupivacaine infiltration would improve pain control and reduce opioid requirements.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-02.
Trial Details
NCT Number NCT07518225
Lead Sponsor Esra Beyler
Collaborators: Baskent University
Conditions Postoperative Pain, Orthognathic Surgery
Enrollment 102 participants
Start Date 2022-09-02
Primary Completion 2025-09-01 (estimated)
Study Completion 2025-09-02 (estimated)
Updated on ClinicalTrials.gov 2026-04-21