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Compression Bandage in Local Infiltration Analgesia Afte Total Knee Arthroplasty

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ClinicalTrials.gov Identifier: NCT00485212
Recruitment Status : Completed
First Posted : June 12, 2007
Last Update Posted : June 12, 2007
Sponsor:
Information provided by:
Hvidovre University Hospital

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

Condition or disease Intervention/treatment Phase
Total Knee Arthroplasty Device: compression bandage Phase 4

Detailed Description:
patients are randomised to receive a compression bandage or a non-compression bandage

Study Design
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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 48 participants
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
Study Start Date : January 2007
Actual Study Completion Date : May 2007

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Knee Replacement
U.S. FDA Resources

Arms and Interventions
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Outcome Measures
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Primary Outcome Measures :
  1. pain, Visual Analogue Scale

Eligibility Criteria
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

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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
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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
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Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

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

Keywords provided by Hvidovre University Hospital:
postoperative pain