Clinical Trials in Turkey / NCT07233785
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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
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| Sivas Cumhuriyet University School of Medicine, Anesthesiology and Reanimation | Sivas | Sivas |
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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