Analgesia for knee arthroscopy: adductor canal block alone vs with BiFeS block

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study compares three analgesic approaches after meniscopathy surgery: adductor canal block (ACB) alone, ACB combined with a BiFeS block, and a control group. The aim is to determine if the BiFeS block adds pain relief while preserving motor function. Participants are adults aged 18-65 with ASA I-III and BMI 18-30, undergoing arthroscopic knee procedures. Analgesic efficacy and safety will be assessed to inform multimodal pain strategies for postoperative recovery.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients aged 18-65 years
* American Society of Anesthesiologists (ASA) score I-II-III
* Body Mass Index (BMI) between 18-30 kg/m2

Exclusion Criteria:

* 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

Where it's running

• Ankara Etlik City Hospital
  Ankara, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Atakan Sezgi
• Email: kansezgi@gmail.com
• Phone: 00905323327000

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.