Actively Recruiting
Comparison of Sciatic, BiFeS, and IPACK Blocks Added to the Adductor Canal Block for Postoperative Pain Control in Primary Total Knee Arthroplasty: A Randomized Controlled Trial
Led by Erzincan University · Updated on 2026-01-13
102
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Postoperative pain after total knee arthroplasty (TKA) can delay recovery, lower patient satisfaction, and increase the need for pain medicine. Researchers are studying three nerve block techniques—sciatic nerve block, Biceps Femoris Short Head (BiFeS) block, and Interspace Between the Popliteal Artery and the Capsule of the posterior Knee (IPACK) block—to see which works best when added to the commonly used adductor canal block. The goal is to find the optimal combination to control pain while preserving leg movement and improving patient satisfaction. This research is a prospective, double-blind, randomized controlled trial including at least 102 adults aged 18 to 75 scheduled for elective unilateral primary TKA. Patients are randomly assigned to receive one of three combinations: adductor canal block plus sciatic nerve block, adductor canal block plus BiFeS block, or adductor canal block plus IPACK block. All nerve blocks use ultrasound guidance and a mixture of local anesthetics. Surgery is performed under spinal anesthesia, and all blocks are done by an experienced anesthesiologist. Participants will be closely monitored during and after surgery. Pain levels will be measured using a visual analog scale at several points within 24 hours postoperatively. Motor function, opioid use, and patient recovery quality will also be assessed. Standard pain medications are given, with tramadol as rescue medication if needed. Data collectors and outcome assessors remain blinded to the treatment groups. The study will run over a 12-month period starting November 2025.
CONDITIONS
Brief Title
Supplementary Nerve Blocks Added to the Adductor Canal Block for Postoperative Pain Management in Primary Total Knee Arthroplasty: A Randomized Controlled Comparison of Sciatic, BiFeS, and IPACK Techniques
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients classified as American Society of Anesthesiologists (ASA) physical status I-III
- Patients undergoing primary total knee arthroplasty
- Patients undergoing unilateral total knee arthroplasty
- Patients between 18 and 75 years of age
You will not qualify if you...
- Patients classified as American Society of Anesthesiologists (ASA) physical status IV or higher
- Patients undergoing revision total knee arthroplasty
- Patients undergoing bilateral total knee arthroplasty
- Patients with neuromuscular disease
- Patients who decline to participate in the study
- Patients with cognitive dysfunction
- Patients with known drug allergies
- Patients with a history of local anesthetic systemic toxicity
- Patients with neurological dysfunction
- Patients with bleeding diathesis
- Pregnant patients
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person) one day before surgery for informed consent and study explanation
Duration - Day of surgery
Participants undergo primary total knee arthroplasty with spinal anesthesia and are randomized to receive a supplementary nerve block (Sciatic, BiFeS, or IPACK) added to the Adductor Canal Block during surgery.
1 visit (in-person) on the day of surgery
Duration - 24 hours post-surgery
Participants are monitored for 24 hours after surgery with pain assessments, motor function evaluations, opioid use tracking, and recovery quality questionnaires.
Pain and motor function assessments at 1, 4, 8, 12, and 24 hours after surgery
Trial Site Locations
Total: 1 location
1
Erzincan Binali Yıldırım Üniversitesi
Erzincan, Merkez, Turkey (Türkiye), 24000
Actively Recruiting
Research Team
M
mustafa somunkıran, anesthesiology resident
F
fethi akyol, Assistant Professor
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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