Efficacy of Adductor Channel Block for anterior cruciate ligament surgery: A prospective double blinded randomized controlled trial

Recruiting

• Conditions: anterior cruciate ligament rupture; 10043237

• Registration Number: NL-OMON51570
• Lead Sponsor: Sint Antonius Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-10-01
• Last Update Posted: 9 April 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 34

Inclusion Criteria

- ASA classification 1-3
- Age >= 18 years
- Anterior cruciate ligament surgery
- General anesthesia
- Informed consent

Exclusion Criteria

- Contraindication to local anesthetics
- Neuromuscular disease

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is postoperative pain (numerical rating score) within the<br /><br>first 24 hours</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints are pain score 48 hours postoperative, motor block result,<br /><br>use of postoperative pain medication including opiates and the use of rescue<br /><br>medication, postoperative pain location, postoperative nausea and vomiting, use<br /><br>of anti-emetics, overall patient satisfaction, contact within 48 hours after<br /><br>surgery with general practicioner or emergency department and adverse events.</p><br>