Clinical Trial

BiFeS vs. iPACK in Postoperative Knee Arthroplasty Analgesia

Recruiting
View on ClinicalTrials.gov →
Summary
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.
Protocol Amendment History 1 change
critical Recruitment opened 2026-04-23
Trial Details
NCT Number NCT07360392
Lead Sponsor Amasya University
Conditions Arthroplasty, Replacement, Knee, Pain, Postoperative, Anesthesia, Regional
Enrollment 88 participants
Start Date 2026-04-20
Primary Completion 2027-03-01 (estimated)
Study Completion 2027-06-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-22