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Clinical Trials/NCT06402110
NCT06402110
Completed
Not Applicable

Femoral Triangle Block Versus Adductor Canal Block for Analgesia After Arthroscopic Anterior Cruciate Ligament Reconstruction: A Randomized Trial

Tanta University1 site in 1 country70 target enrollmentMay 7, 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Femoral Triangle Block
Sponsor
Tanta University
Enrollment
70
Locations
1
Primary Endpoint
Total morphine consumption
Status
Completed
Last Updated
9 months ago

Overview

Brief Summary

The aim of this study is to compare the postoperative analgesic effect of femoral triangle block (FTB) and adductor canal block (ACB)after arthroscopic anterior cruciate ligament (ACL) reconstruction.

Detailed Description

The number of patients undergoing arthroscopic anterior cruciate ligament (ACL) reconstruction has risen over the past decade. ACL reconstruction is associated with moderate to severe postoperative pain leading to hypertension, tachycardia, increased O2 demand, and myocardial stress.

Registry
clinicaltrials.gov
Start Date
May 7, 2024
End Date
April 27, 2025
Last Updated
9 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohammed Said ElSharkawy

Lecturer of Anesthesiology, Surgical Intensive Care and Pain Medicine, Faculty of Medicine, Tanta University, Tanta, Egypt.

Tanta University

Eligibility 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/m
  • Coagulopathy.
  • Infection at site of intervention.
  • Hypersensitive to the study drugs.
  • Chronic analgesic use.
  • Neuromuscular disease.
  • Drug abuse.
  • Cognitive impairment.

Outcomes

Primary Outcomes

Total morphine consumption

Time Frame: 24 hours postoperatively

Rescue analgesia of 3 mg morphine IV will be given if the Numeric Rating Scale (NRS) \> 3 to be repeated after 30 min if pain persists until the NRS \< 4. NRS will be assessed at 2, 4, 6, 12, and 24h postoperatively

Secondary Outcomes

  • Quadriceps strength(24 hours postoperatively)
  • Time of 1st rescue analgesia(24 hours postoperatively)
  • Pain score using Numeric Rating Scale (NRS)(24 hours postoperatively)
  • Patient satisfaction(24 hours postoperatively)

Study Sites (1)

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