Fast-Track vs Conventional for UKA

This study has been completed.
Sponsor:
Information provided by:
Frederiksberg University Hospital
ClinicalTrials.gov Identifier:
NCT00284635
First received: January 31, 2006
Last updated: July 3, 2007
Last verified: July 2007

January 31, 2006
July 3, 2007
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Complete list of historical versions of study NCT00284635 on ClinicalTrials.gov Archive Site
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Fast-Track vs Conventional for UKA
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The purpose of this study is to see if it is possible to discharge patient undergoing a UKA 1 day postoperatively

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Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Unicompartmental Knee Replacement
Procedure: Fast track vs conventional
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
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Inclusion Criteria:

  • UKA, ASA I-II

Exclusion Criteria:

  • medical history of abdominal bleeding
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Denmark
 
NCT00284635
KF-01-231/03
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Frederiksberg University Hospital
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Principal Investigator: arne borgwardt, M.D. Frederiksberg University Hospital
Frederiksberg University Hospital
July 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP