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Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement

NCT01032538 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 99

Last updated 2023-12-01

Study results available
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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.

Conditions

Sponsors & Collaborators

  • South-Eastern Norway Regional Health Authority

    collaborator OTHER

  • Martina Hansen's Hospital

    lead OTHER

Principal Investigators

  • Tor Kjetil Nerhus, MD · Martina Hansens Hospital

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-11-30
Primary Completion
2009-02-28
Completion
2017-02-28

Countries

  • Norway

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01032538 on ClinicalTrials.gov