Ireland
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Comparison of ACB With ACB and BiFeS Combination in Knee Arthroplasty Surgeries

NCT07233785 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2025-11-20
Last updated
2025-11-25

Condition(s) studied

Postoperative Pain ManagementKnee SurgeryKnee Arthroplasty, Total

Investigational drug(s) / intervention(s)

Adductor Canal Block (ACB) OnlyAdductor Canal Block (ACB) + Biceps Femoris Short Head Block (BiFeS)

Adductor Canal Block (ACB) Only: 20 mL of 0.25% bupivacaine

Adductor Canal Block (ACB) + Biceps Femoris Short Head Block (BiFeS): 20 mL of 0.25% bupivacaine

Study summary

The aim is to compare the postoperative analgesic effects of Adductor Canal and Biceps Femoris Short Head Blocks with Adductor Canal Block in patients undergoing Knee Arthroplasty surgery

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients over 18 years of age who underwent percutaneous nephrolithotomy under general anesthesia and were I-II-III according to the American Society of Anesthesiologists (ASA) risk classification were included in the study. Exclusion Criteria: * patients who did not give consent, * patients with coagulopathy, * patients with signs of infection at the block application site, * patients using anticoagulants, * patients with known allergies to any of the study drugs, * patients with unstable hemodynamics, * patients who could not cooperate during postoperative pain assessment * patients who wanted to withdraw from the study, * patients with alcohol and drug addiction, * patients with musculoskeletal abnormalitie

Primary outcome measure(s)

  • 1. Numeric Rating Scale (NRS) Scores — Postoperative 24 hours
    Numerical rating scale is used for pain assessment. The scores of the numerical rating scale changes between 0 to 10 points. 10 points mean "the most severe pain that the patient ever had". 0 point means "there is no pain." Higher scores mean worse outcome.

Trial sites (1)

FacilityCityRegionStatus
Sivas Cumhuriyet University School of Medicine, Anesthesiology and Reanimation Sivas Sivas
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07233785 on ClinicalTrials.gov ↗ ← All trials in Turkey