About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
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.
Disqualifiers
patients who did not give consent,
patients with coagulopathy,
patients with signs of infection at the block application site,
patients using anticoagulants,
Trial design
Parallel
Treatments tested in this trial
Adductor Canal Block (ACB) Only
Procedure/Surgery20 mL of 0.25% bupivacaine
Adductor Canal Block (ACB) + Biceps Femoris Short Head Block (BiFeS)
Procedure/Surgery20 mL of 0.25% bupivacaine
Treatment groups
Trial outcomes
Primary outcomes
1. Numeric Rating Scale (NRS) Scores
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.
Secondary outcomes
Total tramadol consumption
Postoperative total analgesic need was recorded as "milligram" in unit.
Sponsors and contacts
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