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Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

This study has been completed.
Sponsor:
Information provided by:
Hvidovre University Hospital
ClinicalTrials.gov Identifier:
NCT00485212
First received: June 11, 2007
Last updated: NA
Last verified: May 2007
History: No changes posted
  Purpose

purpose: to determine wether a compression bandage prolongs analgesia of local infiltration analgesia after total knee arthroplasty


Condition Intervention Phase
Total Knee Arthroplasty
Device: compression bandage
Phase 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Effect of a Compression Bandage in Local Infiltration Analgesia After Total Knee Arthroplasty

Resource links provided by NLM:


Further study details as provided by Hvidovre University Hospital:

Primary Outcome Measures:
  • pain, Visual Analogue Scale

Enrollment: 48
Study Start Date: January 2007
Study Completion Date: May 2007
Detailed Description:

patients are randomised to receive a compression bandage or a non-compression bandage

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • scheduled for total knee arthroplasty
  • speak and understand Danish

Exclusion Criteria:

  • severe obesity
  • allergies to local anaesthetics
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00485212

Locations
Denmark
Hvidovre Hospital
Hvidovre, Denmark, 2650
Sponsors and Collaborators
Hvidovre University Hospital
Investigators
Principal Investigator: Lasse Andersen, MD Hvidovre University Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00485212     History of Changes
Other Study ID Numbers: KF01327078
Study First Received: June 11, 2007
Last Updated: June 11, 2007
Health Authority: Denmark: The Regional Committee on Biomedical Research Ethics

Keywords provided by Hvidovre University Hospital:
postoperative pain

ClinicalTrials.gov processed this record on November 25, 2014