Clinical Trial

Comparison of the Analgesic Efficacy of Adductor Canal Block Versus Adductor Canal Plus Biceps Femoris Short Head Block in Patients Undergoing Knee Arthroscopy

Study acronym: bifes knee
Completed
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Summary
This prospective, randomized, controlled, and multicenter clinical study aims to compare the postoperative analgesic efficacy of two regional anesthesia techniques commonly used in knee arthroscopy: adductor canal block (ACB) and combined adductor canal block plus biceps femoris short head (ACB+BiFeS) block. The study will evaluate postoperative pain control, opioid consumption, adverse effects, hospital stay, and patient satisfaction. Findings will help determine the most effective and safe method for postoperative analgesia in knee arthroscopy patients.
Protocol Amendment History 1 change
critical Trial completed 2026-04-08
Trial Details
NCT Number NCT07242339
Lead Sponsor Kanuni Sultan Suleyman Training and Research Hospital
Conditions Postoperative Pain Management
Enrollment 50 participants
Start Date 2025-11-20
Primary Completion 2026-04-03 (estimated)
Study Completion 2026-04-03 (estimated)
Updated on ClinicalTrials.gov 2026-04-07