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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Adductor canal block | Before anterior cruciate ligament surgery an adductor canal block will be placed using ultrasound. |
| DRUG | Levobupivacaine | Levobupivacaine |
| DRUG | Placebo | 10 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.