N/A
N=99
Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement
Osteoarthritis
Bottom Line
View on ClinicalTrials.gov: NCT01032538 ↗Enrolled (actual)
99
Serious AEs
5.2%
Results posted
Jan 2015
Primary outcome: Primary: Knee Injury and Osteoarthritis Outcome Score — 85.5; 88.2 units on a scale
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Adult, Older Adult · 50+ yrs
- Sex
- All
- Sponsor
- Vestre Viken Hospital Trust
- Primary completion
- Feb 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Knee Injury and Osteoarthritis Outcome Score |
— | — |
| SECONDARY Range of Motion |
128 | — |
| SECONDARY Oxford Knee Score |
— | — |
| SECONDARY UCLA Score |
— | — |
| SECONDARY Knee Injury and Osteoarthritis Outcome Score |
— | — |
| SECONDARY Oxford Knee Score |
— | — |
Summary
The objective of this prospective study is to determine (1) the time course of patient-relevant functional outcome evaluated by the Knee injury and Osteoarthritis Outcome Score (KOOS) and (2) the time course of range of motion (ROM) the first six years following Oxford Medial Unicondylar Knee prosthesis. Improvement of patient self-reported pain and daily function during the study period, are of particular interest.
Eligibility Criteria
Inclusion Criteria
- patients with medial knee osteoarthritis
- admitted for unicondylar knee replacement
- age 50-80 years
Exclusion criteria
- rheumatoid arthritis
- previous knee infection
Data sourced from ClinicalTrials.gov (NCT01032538). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.