Knee Replacement Clinical Trials

Clinical trials related to Knee Replacement Procedure

Comparison of Analgesic Efficacy of Infiltration Between the Popliteal Artery and Capsule of the Knee (IPACK) Versus Biceps Femoris Short Head Block Combined With Adductor Canal Block in Total Knee Arthroplasty

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Total knee arthroplasty (TKA) is associated with severe postoperative pain that delays mobilization, prolongs hospital stay, and reduces patient satisfaction. Regional analgesia techniques have gained prominence due to their opioid-sparing effects and favorable complication profiles compared to general anesthesia. While adductor canal block (ACB) effectively manages anterior knee pain with preserved motor function, posterior knee pain remains a challenge. IPACK (Infiltration between the Popliteal Artery and Capsule of the Knee) and the Biceps Femoris Short Head (BiFeS) block are techniques targeting posterior capsule innervation without causing motor block.This prospective study aims to compare the postoperative analgesic efficacy of ultrasound-guided ACB+IPACK versus ACB+BiFeS block combinations in patients undergoing TKA under spinal anesthesia. Patients (ASA I-III, age 18-80, BMI ≤35) will be randomized into two groups (n=39 each). Primary outcomes include NRS pain scores at rest and on movement, and opioid consumption at 0, 1, 3, 6, 12, 18, and 24 hours postoperatively. Secondary outcomes include time to first mobilization, motor block incidence, quadriceps muscle strength assessment, PONV, and quality of recovery (QoR-15).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Scheduled for primary total knee arthroplasty surgery

• ASA physical status classification I-III

• Hemodynamically stable

• Age ≥ 18 years and ≤ 80 years

• BMI ≤ 35 kg/m²

• Signed written informed consent form

Locations
Other Locations
Turkey
Hitit University
RECRUITING
Çorum
Contact Information
Primary
Merve YAGIZ BALDIRAN, MD
merveyagiz-1@hotmail.com
+905432835144
Backup
Arzu AKDAGLI EKICI, MD
akekici@gmail.com
+905057516387
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2026-11-01
Participants
Target number of participants: 78
Treatments
Active_comparator: ACB+IPACK Group
ACB+IPACK Group:~Patients receiving ultrasound-guided adductor canal block (15 mL of 0.25% bupivacaine) combined with IPACK block (25 mL of 0.25% bupivacaine) for postoperative analgesia following total knee arthroplasty under spinal anesthesia.
Active_comparator: ACB+BiFeS Group
ACB+BiFeS Group:~Patients receiving ultrasound-guided adductor canal block (15 mL of 0.25% bupivacaine) combined with Biceps Femoris Short Head block (25 mL of 0.25% bupivacaine) for postoperative analgesia following total knee arthroplasty under spinal anesthesia.
Related Therapeutic Areas
Sponsors
Leads: Hitit University

This content was sourced from clinicaltrials.gov

Similar Clinical Trials