Fast-Track vs Conventional for UKA

Unicompartmental Knee Replacement Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00284635
• Other study ID #: KF-01-231/03
• Status: Completed
• Phase: Phase 4
• First received: January 31, 2006
• Last updated: July 3, 2007

Study information

• Verified date: July 2007
• Source: Frederiksberg University Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Denmark: Ethics Committee
• Study type: Interventional

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• UKA, ASA I-II

Exclusion Criteria:

• medical history of abdominal bleeding

Study Design

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

Related Conditions & MeSH terms

• Unicompartmental Knee Replacement

Intervention

Procedure:
• Fast track vs conventional

Locations

Country	Name	City	State
Denmark	Frederiksberg University Hospital	Copenhagen	Frederiksberg C

Sponsors (1)

Lead Sponsor	Collaborator
Frederiksberg University Hospital

Country where clinical trial is conducted

Denmark,