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

U

University Ghent

Status

Completed

Conditions

Postoperative Pain

Treatments

Device: Lockit-Plus
Device: Tegaderm dressing
Device: Epi-Fix dressing

Study type

Interventional

Funder types

Other

Identifiers

NCT00764283
2008/278

Details and patient eligibility

About

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.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

200 participants in 3 patient groups

1
Experimental group
Description:
Tegaderm dressing
Treatment:
Device: Tegaderm dressing
2
Active Comparator group
Description:
Epi-Fix dressing
Treatment:
Device: Epi-Fix dressing
3
Active Comparator group
Description:
Lockit-Plus dressing
Treatment:
Device: Lockit-Plus

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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