CompletedNot Applicable

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

Turkey (Türkiye)50 participantsStarted 2025-11-20

Plain-language 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.

Who can participate

Age range18 Years

SexALL

See this in plain English?

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

Inclusion Criteria: * Age ≥ 18 years * ASA physical status I-III * Scheduled for elective knee arthroscopy under spinal anesthesia * Ability to provide written informed consent Exclusion Criteria: * Coagulopathy or bleeding diathesis * Current use of anticoagulant therapy * Known allergy or contraindication to local anesthetics used in the study * History of diabetes mellitus with neuropathy or other neuropathic disorders * Contraindications to regional anesthesia techniques * Refusal to participate

What they're measuring

Total Opioid Consumption (Tramadol, mg)

Timeframe: 24 hours

Trial details

NCT IDNCT07242339

SponsorKanuni Sultan Suleyman Training and Research Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-04-03

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