Actively Recruiting
Comparison of Analgesic Effects of Adductor Canal Block Versus Adductor Canal Block Combined With BiFeS (Biceps Femoris Short Head) Block in Meniscopathy Surgery
Led by Ankara Etlik City Hospital · Updated on 2026-05-29
135
Participants Needed
1
Research Sites
2 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Meniscopathy surgeries often cause moderate pain after the operation, especially during early movement and rehabilitation. Poor pain control after surgery can slow recovery, delay walking, increase the need for opioid pain medication, and cause opioid-related side effects. Researchers are comparing two types of nerve blocks to improve pain relief after arthroscopic knee surgery: the commonly used adductor canal block (ACB) and a combination of ACB with a newer biceps femoris short head (BiFeS) block that targets additional nerves around the knee. The study compares three groups of patients undergoing meniscopathy surgery. One group receives an adductor canal block using 10 ml of 0.25% bupivacaine under ultrasound guidance. Another group receives the same adductor canal block plus a BiFeS block using 20 ml of 0.25% bupivacaine, also guided by ultrasound. The control group does not receive any regional nerve block. All groups receive standard postoperative pain medicines including paracetamol and dexketoprofen. Participants will be monitored on the day of surgery for pain levels and opioid use. Researchers will measure pain scores and total morphine consumption during the first 24 hours after surgery. Ultrasound imaging confirms proper anesthetic placement during nerve blocks. The study is randomized and single-blinded, aiming to find which approach provides better pain relief while preserving muscle strength. The trial lasts from the surgery day through the initial postoperative period for recovery assessment.
CONDITIONS
Brief Title
Comparison of Analgesic Effects of ACB Versus ACB Combined With BiFeS Block in Meniscopathy Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 18-65 years
- American Society of Anesthesiologists (ASA) score I-II-III
- Body Mass Index (BMI) between 18-30 kg/m2
You will not qualify if you...
- Patients under 18 and over 65 years of age
- ASA score IV and above
- Patients with a history of bleeding diathesis
- BMI below 18 or above 30 kg/m2
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)
Duration - On the operation day
Participants receive either adductor canal block alone, adductor canal block combined with BiFeS block, or no regional block during meniscopathy surgery, along with postoperative multimodal analgesia.
1 visit (in-person)
Duration - 24 hours after surgery
Postoperative monitoring of pain scores and morphine consumption during the first 24 hours after surgery.
1 follow-up visit (in-person)
Trial Site Locations
Total: 1 location
1
Ankara Etlik City Hospital
Ankara, Turkey (Türkiye)
Actively Recruiting
Research Team
A
Atakan Sezgi
M
Musa Zengin
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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