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Main
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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. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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17 October 2012 |
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Main ID: |
NCT01032538 |
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Date of registration:
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14/12/2009 |
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Primary sponsor: |
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Public title:
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Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement
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Scientific title:
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Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement - A Prospective Longitudinal Study With Repetitive Measures of KOOS in 100 Patients |
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Date of first enrolment:
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November 2003 |
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Target sample size:
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100 |
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Recruitment status: |
Active, not recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01032538 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Countries of recruitment
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Norway
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Contacts
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Name:
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Tor Kjetil Nerhus, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Martina Hansens Hospital |
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Key inclusion & exclusion criteria
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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
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Health Condition(s) or Problem(s) studied
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Osteoarthritis
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Primary Outcome(s)
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Knee injury and Osteoarthritis Outcome Score
[Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
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Secondary Outcome(s)
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Knee injury and Osteoarthritis Outcome Score
[Time Frame: 6 years and 10 years postoperatively]
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Oxford knee score
[Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
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Range of Motion
[Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
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UCLA score
[Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively]
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Secondary ID(s)
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19441 (NSD)
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TKN-002
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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