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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT01032538
Date of registration: 14/12/2009
Primary sponsor: Martina Hansen's Hospital
Public title: Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement
Scientific title: Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement - A Prospective Longitudinal Study With Repetitive Measures of KOOS in 100 Patients
Date of first enrolment: November 2003
Target sample size: 100
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT01032538
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Prospective  
Countries of recruitment
Norway
Contacts
Name:   Tor Kjetil Nerhus, MD
Address: 
Telephone:
Email:
Affiliation:  Martina Hansens Hospital
Key inclusion & exclusion criteria

Inclusion Criteria:

- patients with medial knee osteoarthritis

- admitted for unicondylar knee replacement

- no rheumatoid arthritis

- no previous knee infection

- age 50-80 years



Age minimum: 50 Years
Age maximum: 80 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Osteoarthritis
Intervention(s)
Primary Outcome(s)
Knee injury and Osteoarthritis Outcome Score [Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
Secondary Outcome(s)
Knee injury and Osteoarthritis Outcome Score [Time Frame: 6 years and 10 years postoperatively]
Oxford knee score [Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
Range of Motion [Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
UCLA score [Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
Secondary ID(s)
19441 (NSD)
TKN-002
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
South-Eastern Norway Regional Health Authority
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