Postoperative analgesia with continuous epidural bupivacaine/sufentanil versus bupivacaine/morphine in patients undergoing major surgery.

Phase 4

Completed

• Conditions: pijnbehandeling; analgesia

• Registration Number: NL-OMON33682
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 530

Inclusion Criteria

All patients > - 18 years old, scheduled for major surgery and indicated for epidural catheter.

Exclusion Criteria

No dutch speaking, mental disability, allergy to one of the study medications. Pregnancy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>-The pain scores of the patient on the Numerical Rating Scale (NRS) during the<br /><br>first<br /><br>72 hours after surgery.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>-Registration of side-effects: pruritus, nausea and vomiting.<br /><br>-Registration of adverse effects: respiratory depression, sedation and motor<br /><br>block.<br /><br>-The quality of pain relief by the patient.</p><br>