Postoperative analgesia with continuous epidural bupivacaine/sufentanil versus bupivacaine/morphine in patients scheduled for major surgery. - bupisuf

• Conditions: Pain scores and side-effects of the epidural analgesia; MedDRA version: 9.1Level: LLTClassification code 10033371Term: Pain

• Registration Number: EUCTR2007-005275-33-NL

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2009-02-17
• Last Update Posted: 19 March 2012

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

All patients > - 18 years old, scheduled for major surgery and indicated for epidural catheter.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

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

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: Pain scores;Secondary Objective: Side-effects: nausea, vomiting, pruritus, sedation, motorblok and patient satisfaction.;Primary end point(s): VAS pain scores.