Clinical trial Recruiting at 1 site Interventional Ages 18 to 72

Comparing pain relief methods after knee surgery

Official title: Comparison of the Effectiveness of Adductor Canal Block and Genicular Nerve Block on Postoperative Pain and Analgesic Use in Arthroscopic Knee Surgeries

Run by Başakşehir Çam & Sakura City Hospital · NCT06909851 · Data updated 2026-11-12

This study is testing which pain relief method, Adductor Canal Block or Genicular Nerve Block, works better for people aged 18-72 after knee surgery.

Quick facts

Study typeInterventional
Ages18 Years to 72 Years
SexAll
Enrollment68 (estimated)
SponsorBaşakşehir Çam & Sakura City Hospital
Government
Locations1 site (Istanbul)
StatusRecruiting
StartedMarch 10, 2025
Main results expectedAugust 31, 2025
Study endsSeptember 30, 2025
Registry record updatedApril 4, 2025
Trial IDNCT06909851 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18-72 undergoing arthroscopic knee surgery who are suitable for regional anesthesia.

Probably not a fit

Patients undergoing surgery under general anesthesia or those with chronic analgesic use may not benefit from this study.

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

What this trial studies

This prospective randomized study compares the effectiveness of two pain relief techniques, Adductor Canal Block (ACB) and Genicular Nerve Block (GNB), for patients aged 18-72 undergoing arthroscopic knee surgery under spinal anesthesia. The study aims to evaluate postoperative pain levels, opioid consumption, and patient satisfaction over a 24-hour period following surgery. Participants will be monitored for pain scores and overall satisfaction to determine which method provides better analgesia.

Why it matters

Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing knee surgery, potentially reducing opioid use.

How similar studies have gone: Previous studies have shown promising results with similar nerve block techniques for postoperative pain management, indicating potential success for this approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Voluntary willingness to participate in the study.
* Patients undergoing arthroscopic knee surgery (meniscus, ACL, arthroscopic intervention etc).
* ASA I-II-III classification.
* Aged between 18-72 years.
* No contraindications for regional anesthesia, and deemed suitable for regional anesthesia by the anesthesiologist.
* Undergoing surgery under spinal anesthesia.
* Fully oriented and able to cooperate.

Exclusion Criteria:

* Undergoing surgery under general anesthesia.
* Chronic analgesic use.
* Presence of an active infection at the procedure site.
* Outside the appropriate age range.
* Inability to comply with postoperative pain/NRS follow-ups.
* ASA IV-V classification.
* Non-voluntary patients.
* Pregnancy.

Where it's running

  • Başakşehir Çam & Sakura City Hospital
    Istanbul, Turkey (Türkiye)
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.