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 type | Interventional |
|---|---|
| Ages | 18 Years to 72 Years |
| Sex | All |
| Enrollment | 68 (estimated) |
| Sponsor | Başakşehir Çam & Sakura City Hospital Government |
| Locations | 1 site (Istanbul) |
| Status | Recruiting |
| Started | March 10, 2025 |
| Main results expected | August 31, 2025 |
| Study ends | September 30, 2025 |
| Registry record updated | April 4, 2025 |
| Trial ID | NCT06909851 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
- Study coordinator: Muzaffer Gencer
- Email: dr.m.gencer07@gmail.com
- Phone: +905059436459
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Dexa vs Dexmedetomidine with Bupivacaine in TAP Block for Laparotomy Analgesia
This study tests whether adding dexamethasone or dexmedetomidine to bupivacaine in a TAP block improves postoperative pain control after laparotomy.
-
Autonomic Nerve Blockade to Reduce Pain and Nausea After Bariatric Surgery
This study tests whether an autonomic nerve block given during bariatric surgery can lessen pain and nausea and decrease the need for anti-nausea and pain medicines in the first 72 hours after sleeve gastrectomy or gastric bypass.
-
Using the Nociception Level Index to guide opioid dosing during combined regional and general anesthesia
This trial tests whether using a Nociception Level Index (NOL) monitor to guide opioid dosing during combined general and regional anesthesia can reduce opioid use and side effects for adults having elective trauma or orthopedic surgery.
-
Comparing ketamine delivery methods for postoperative pain management in orthopedic surgery
This study is testing whether giving ketamine through an IV or a patient-controlled pump works better for managing pain after major orthopedic surgery in adults.
-
Comparing pain relief methods after lumbar fusion surgery
This study tests whether a new way of giving local anesthesia during lumbar fusion surgery can help patients feel less pain and use fewer opioids compared to the traditional method.
-
Smart opioid dispenser and app for patients having a one-level lumbar discectomy or laminectomy
This test tries a locked opioid-dispensing device plus a smartphone app to help adults having a one-level lumbar discectomy or laminectomy who are opioid-naive or occasional users take oxycodone more safely after discharge.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.