Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Fast-Track vs Conventional for UKA
This study has been completed.
Sponsored by: Frederiksberg University Hospital
Information provided by: Frederiksberg University Hospital
ClinicalTrials.gov Identifier: NCT00284635
  Purpose

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


Condition Intervention Phase
Unicompartmental Knee Replacement
 Procedure: Fast track vs conventional
 Phase IV

U.S. FDA Resources
Study Type: Interventional
Study Design: Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • UKA, ASA I-II

Exclusion Criteria:

  • medical history of abdominal bleeding
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00284635

Locations
Denmark, Frederiksberg C
Frederiksberg University Hospital
Copenhagen, Frederiksberg C, Denmark, 2000
Sponsors and Collaborators
Frederiksberg University Hospital
Investigators
Principal Investigator: arne borgwardt, M.D. Frederiksberg University Hospital
  More Information

Study ID Numbers: KF-01-231/03
Study First Received: January 31, 2006
Last Updated: July 3, 2007
ClinicalTrials.gov Identifier: NCT00284635  
Health Authority: Denmark: Ethics Committee

ClinicalTrials.gov processed this record on January 16, 2009



U.S. National Library of Medicine,  Contact Help Desk
U.S. National Institutes of Health,  U.S. Department of Health & Human Services,
USA.gov,  Copyright,  Privacy,  Accessibility,  Freedom of Information Act

U.S. National Institutes of Health U.S. National Library of Medicine U.S. Department of Health & Human Services