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Study identifier: NCT06909851 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Comparison of Pain Relief After Arthroscopic Knee Surgery: Adductor Canal Block and Genicular Nerve Block

Condition: Opioid Use · Pain Postoperative · Arthroscopic Knee Surgeries  ·  Sponsor: Başakşehir Çam & Sakura City Hospital

PhaseNA
Planned participants68
Who can joinAll sexes, 18 Years to 72 Years
Healthy volunteersYes

About this study

This prospective randomized study aims to compare the analgesic efficacy of Adductor Canal Block (ACB) and Genicular Nerve Block (GNB) groups to relieve postoperative pain in participants between ages of 18-72 undergoing arthroscopic knee surgery under spinal anesthesia. The main question it aims to answer is: To demonstrate whether Adductor Canal Block or Genicular Nerve Block is more effective in postoperative analgesia in patients undergoing arthroscopic knee surgery based on pain scores, opioid consumption and patient satisfaction. Arthroscopic knee surgeries cause severe pain especially with movement in the post-operative period. After surgery, the movements of the participants are severely restricted because of pain, which increases the possibility of complications and postpones post-operative knee exercises. In this study, the participants' pain status, VAS score, opioid consumption and patient satisfaction will be measured with a simple scoring system for 24 hours at predetermined time points and then compared. Both types of blocks have pain-relieving effects. This study will only investigate which one is more effective in reducing pain, and there will be no deficiency in relieving the pain of the participants.

This description comes directly from the study's public registry record.

Talk to the study team

MUZAFFER GENCER  ·  +905059436459  ·  dr.m.gencer07@gmail.com

SİNAN ANAŞ  ·  +905314220762  ·  tharkunbalrogs@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Başakşehir Çam & Sakura City HospitalIstanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT06909851