Comparing two pain relief methods after knee ligament surgery
Femoral Triangle Block Versus Adductor Canal Block for Analgesia After Arthroscopic Anterior Cruciate Ligament Reconstruction: A Randomized Trial
NA · Tanta University · NCT06402110
This study is testing which of two pain relief methods works better for people recovering from knee ligament surgery.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 70 (estimated) |
| Ages | 21 Years to 65 Years |
| Sex | All |
| Sponsor | Tanta University (other) |
| Locations | 1 site (Tanta, El-Gharbia) |
| Trial ID | NCT06402110 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of two different pain relief techniques, the femoral triangle block (FTB) and the adductor canal block (ACB), in patients undergoing arthroscopic anterior cruciate ligament (ACL) reconstruction. The focus is on assessing postoperative pain management, as ACL surgeries often result in significant pain that can lead to various complications. By evaluating the analgesic effects of these two blocks, the study seeks to determine which method provides better pain control for patients after surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 21 to 65 who are scheduled for elective ACL reconstruction and are classified as ASA physical status I or II.
Not a fit: Patients undergoing revisional surgery, those with a BMI over 35, or individuals with coagulopathy or other specified exclusions may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management strategies for patients undergoing ACL reconstruction.
How similar studies have performed: Previous studies have shown varying success with similar analgesic techniques, but this specific comparison of FTB and ACB in ACL reconstruction is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age from 21 to 65 years. * Both sexes. * American Society of Anesthesiologists (ASA) physical status I and II. * Undergoing elective arthroscopic Anterior Cruciate Ligament (ACL) reconstruction. Exclusion Criteria: * Revisional surgery. * Body mass index (BMI) \>35kg/m2. * Coagulopathy. * Infection at site of intervention. * Hypersensitive to the study drugs. * Chronic analgesic use. * Neuromuscular disease. * Drug abuse. * Cognitive impairment.
Where this trial is running
Tanta, El-Gharbia
- Tanta University — Tanta, El-Gharbia, Egypt (RECRUITING)
Study contacts
- Study coordinator: Mohammed S Elsharkawy, MD
- Email: mselsharkawy@med.tanta.edu.eg
- Phone: 00201148207870
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Femoral Triangle Block, Adductor Canal Block, Anterior Cruciate Ligament Reconstruction