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Clinical Trials/NCT00764283
NCT00764283
Completed
Not Applicable

The Prevention of Postoperative Epidural Catheter Migration: a Comparison of Three Types of Dressing

University Ghent1 site in 1 country200 target enrollmentNovember 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
University Ghent
Enrollment
200
Locations
1
Primary Endpoint
Epidural catheter migration from insertion till removal
Status
Completed
Last Updated
17 years ago

Overview

Brief Summary

Three types of dressing will be compared to prevent postoperative epidural catheter migration. Patients will be randomised to have a Tegaderm dressing, an Epi-fix dressing or a Lockit-Plus dressing to secure the epidural catheter for postoperative analgesia. The length of the epidural catheter visible at the patient's skin surface will be recorded after insertion and every day until removal. The integrity of the dressing and problems with analgesia will also be recorded.

Registry
clinicaltrials.gov
Start Date
November 2008
End Date
March 2009
Last Updated
17 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • All patients who receive a lumbar epidural catheter for patient controlled analgesia will be included after informed consent
  • 18 years or older

Exclusion Criteria

  • Patients who did not sign an informed consent

Outcomes

Primary Outcomes

Epidural catheter migration from insertion till removal

Time Frame: Until removal of the epidural catheter

Secondary Outcomes

  • Problems of analgesia during Patient Controlled Epidural Analgesia(Until removal of the epidural catheter)
  • Body Mass Index(Until removal of the epidural catheter)
  • The integrity of the dressing(Until removal of the epidural catheter)
  • The comfort of the dressing(Until removal of the epidural catheter)

Study Sites (1)

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