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
  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 4

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label

Further study details as provided by Frederiksberg University Hospital:

  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 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

No publications provided

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

ClinicalTrials.gov processed this record on April 17, 2014