Clinical Trials Directory

Trials / Completed

CompletedNCT05532618

Efficacy of Adductor Canal Block for Anterior Cruciate Ligament Surgery

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
34 (actual)
Sponsor
St. Antonius Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREAdductor canal blockBefore anterior cruciate ligament surgery an adductor canal block will be placed using ultrasound.
DRUGLevobupivacaineLevobupivacaine
DRUGPlacebo10 ml of sodium chloride 0.9%

Timeline

Start date
2022-08-01
Primary completion
2023-08-01
Completion
2023-08-01
First posted
2022-09-08
Last updated
2023-09-13

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT05532618. Inclusion in this directory is not an endorsement.