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Local Infiltration Analgesia vs Adductor Canal Block for Analgesia After Anterior Cruciate Ligament Reconstruction

Phase 4
Completed
Conditions
Rupture of Anterior Cruciate Ligament
Infiltration
Regional Anesthesia Morbidity
Interventions
Registration Number
NCT02524652
Lead Sponsor
Centre Hospitalier Universitaire Vaudois
Brief Summary

Early rehabilitation after anterior cruciate ligament reconstruction is of paramount importance and requires optimal pain control based on a multimodal concept, including injection of local anaesthetics. Regarding this latter, different options have emerged recently such as the adductor canal block, performed before the surgery by the anaesthesiologist or the infiltration of the articulation performed by the surgeon at the of the intervention. No trial has compared these two approaches. As practice of medicine should be based on evidence, we decided to undertake this randomised controlled trial where we compared the adductor canal block with the local infiltration analgesia technique in terms of pain and functional outcomes

Detailed Description

Patients scheduled to undergo anterior cruciate ligament reconstruction under general anaesthesia will be randomly allocated to two groups: local infiltration analgesia or adductor canal block.

The local infiltration analgesia will be performed by the surgeon at the end of surgery with 20 mLs of ropivacaine 0.5%. The adductor canal block will be performed by the anaesthesiologist under ultrasound guidance after the surgery, before awaking the patient, using the same solution (20 mLs ropivacaine 0.5%)

Postoperative analgesia will include intravenous patient-controlled analgesia of morphine (settings 1 mg/ml, 2 ml/10 minutes, 40 mg/4 hours), ibuprofen (3x400 mg) and acetaminophen (4x1000 mg).

A research assistant and a physiotherapist, both blinded to the group allocation, will collect pain and rehabilitation data, respectively.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
104
Inclusion Criteria
  • patients from 18 to 50 years old scheduled to undergo anterior cruciate ligament reconstruction
Exclusion Criteria
  • peripheral neuropathy
  • pre-existing femoral neuropathy
  • diabetes mellitus
  • alcoholism
  • drug addiction
  • cancer with chemotherapy
  • chronic pain state

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Adductor canal blockRopivacaine 0.5% 20 mLsInjection of local anaesthetics under ultrasound guidance in the adductor canal by the anaesthesiologist after the surgery, before awaking the patient.
Local infiltration analgesiaRopivacaine 0.5% 20 mLsInfiltration of the knee by the surgeon with local anaesthetics under general anaesthesia.
Primary Outcome Measures
NameTimeMethod
Total morphine consumption (mg)24 h postoperatively
Secondary Outcome Measures
NameTimeMethod
Total morphine consumption (mg)72 h postoperatively
Pain scores (numeric rating scale, 0-10) at rest and on movement72 h postoperatively
Postoperative nausea and vomiting (yes/no)72 h postoperatively
Pruritus (yes/no)72 h postoperatively
Active flexion72 h postoperatively

Flexion of the knee by the patient measured in degrees

Distance walked (meters)72 h postoperatively
Quadriceps muscle strength (numeric scale, 1-5)72 h postoperatively
Anterior Cruciate Ligament - Return to Sport after Injury scale4 months postoperatively
Anterior cruciate ligament -Return to Sport after Injury scale8 months postoperatively
International Knee Documentation Committee score8 months postoperatively

Trial Locations

Locations (1)

Department of Anesthesia, Centre Hospitalier Universitaire Vaudois and University of Lausanne

🇨🇭

Lausanne, Vaud, Switzerland

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