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Fast-Track vs Conventional for UKA

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.
 
ClinicalTrials.gov Identifier: NCT00284635
Recruitment Status : Completed
First Posted : February 1, 2006
Last Update Posted : July 4, 2007
Sponsor:
Information provided by:
Frederiksberg University Hospital

Brief Summary:
The purpose of this study is to see if it is possible to discharge patient undergoing a UKA 1 day postoperatively

Condition or disease Intervention/treatment Phase
Unicompartmental Knee Replacement Procedure: Fast track vs conventional Phase 4

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Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)




Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • UKA, ASA I-II

Exclusion Criteria:

  • medical history of abdominal bleeding

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): NCT00284635


Locations
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Denmark
Frederiksberg University Hospital
Copenhagen, Frederiksberg C, Denmark, 2000
Sponsors and Collaborators
Frederiksberg University Hospital
Investigators
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Principal Investigator: arne borgwardt, M.D. Frederiksberg University Hospital
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ClinicalTrials.gov Identifier: NCT00284635    
Other Study ID Numbers: KF-01-231/03
First Posted: February 1, 2006    Key Record Dates
Last Update Posted: July 4, 2007
Last Verified: July 2007