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Study identifier: NCT07360392 Synced from ClinicalTrials.gov · August 03, 2026
● Recruiting

BiFeS vs. iPACK in Postoperative Knee Arthroplasty Analgesia

Condition: Arthroplasty, Replacement, Knee · Pain, Postoperative · Anesthesia, Regional  ·  Sponsor: Amasya University

PhaseNA
Planned participants88
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The Biceps Femoris Short Head (BiFeS) block is a new fascial plane block technique targeting the sensory innervation of the posterolateral capsule of the knee while preserving motor function. The aim of this study is to evaluate the postoperative analgesic efficacy of the BiFeS block combined with the adductor canal block (ACB) in patients undergoing total knee arthroplasty, compared to ACB + iPACK block. The study is planned as a prospective, randomized, double-blind, parallel two-group trial. Patients will be randomized in a 1:1 ratio to receive ACB + iPACK (Group A) or ACB + BiFeS (Group B). Postoperative pain scores (VAS), opioid consumption, early mobilization, and quality of recovery (QoR-15) outcomes will be compared.

This description comes directly from the study's public registry record.

Talk to the study team

Bülent M Çam, MD  ·  +90 534 8156011  ·  bulentmericcam@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Amasya University Sabuncuoğlu Şerefeddin Training and Research HospitalAmasya, Turkey (Türkiye)Recruiting

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