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

Last updated: March 27, 2025
Sponsor: Başakşehir Çam & Sakura City Hospital
Overall Status: Active - Recruiting

Phase

N/A

Condition

Drug Use

Treatment

Adductor Canal Block (ACB)

Genicular Nerve Block (GNB)

Clinical Study ID

NCT06909851
BSH-ANES-SA-01
  • Ages 18-72
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

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.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Voluntary willingness to participate in the study.

  • Patients undergoing arthroscopic knee surgery (meniscus, ACL, arthroscopicintervention etc).

  • ASA I-II-III classification.

  • Aged between 18-72 years.

  • No contraindications for regional anesthesia, and deemed suitable for regionalanesthesia by the anesthesiologist.

  • Undergoing surgery under spinal anesthesia.

  • Fully oriented and able to cooperate.

Exclusion

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.

Study Design

Total Participants: 68
Treatment Group(s): 2
Primary Treatment: Adductor Canal Block (ACB)
Phase:
Study Start date:
March 10, 2025
Estimated Completion Date:
September 30, 2025

Connect with a study center

  • Başakşehir Çam & Sakura City Hospital

    İ̇stanbul,
    Turkey

    Active - Recruiting

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