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Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00485212
First Posted: June 12, 2007
Last Update Posted: June 12, 2007
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Hvidovre University Hospital
  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
Intervention Model: Parallel Assignment
Masking: None (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

Information from the National Library of Medicine

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, Learn About Clinical Studies.


Ages Eligible for Study:   Child, Adult, Senior
Sexes Eligible for Study:   All
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
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): 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

ClinicalTrials.gov Identifier: NCT00485212     History of Changes
Other Study ID Numbers: KF01327078
First Submitted: June 11, 2007
First Posted: June 12, 2007
Last Update Posted: June 12, 2007
Last Verified: May 2007

Keywords provided by Hvidovre University Hospital:
postoperative pain