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Efficacy of Adductor Canal Block for Anterior Cruciate Ligament Surgery — DUAL  

Anterior Cruciate Ligament Injuries Clinical Trial

Official title:
Efficacy of Adductor Canal Block for Anterior Cruciate Ligament Surgery: A Prospective Double Blinded Randomized Controlled Trial

Clinical Trial Summary

The goal of this study is to objectify the postoperative pain level, the use of opiates and postoperative nausea and vomiting after adding the adductor canal block to the standard pain regiment after anterior cruciate ligament surgery

Clinical Trial Description

Patients scheduled for anterior cruciate ligament surgery will be randomized in an intervention and control group following informed consent. Before surgery, patients will receive an adductor canal bock with Levobupivacaine (intervention group) or 0.9% saline (control group). Following surgery, pain intensity, analgesic consumption and pain satisfaction will be recorded bij patients in a diary for 48 hours. ;

Study Design

Related Conditions & MeSH terms

  • Anterior Cruciate Ligament Injuries
Clinical Trial Details
NCT number NCT05532618
Study type Interventional
Source St. Antonius Hospital
Contact
Status Completed
Phase N/A
Start date August 1, 2022
Completion date August 1, 2023
View Details
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