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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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 September 18, 2014