Skip to main content
Clinical Trials/NCT01032538
NCT01032538
Completed
Not Applicable

Time-dependent Improvement of Functional Outcome Following Oxford Medial Unicondylar Knee Replacement - A Prospective Longitudinal Study With Repetitive Measures of KOOS in 100 Patients

Martina Hansen's Hospital3 sites in 1 country99 target enrollmentNovember 2003
ConditionsOsteoarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis
Sponsor
Martina Hansen's Hospital
Enrollment
99
Locations
3
Primary Endpoint
Knee Injury and Osteoarthritis Outcome Score
Status
Completed
Last Updated
2 years ago

Overview

Brief 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.

Detailed Description

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. Thats it!

Registry
clinicaltrials.gov
Start Date
November 2003
End Date
February 2017
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Martina Hansen's Hospital
Responsible Party
Principal Investigator
Principal Investigator

Tor Kjetil Nerhus

Consultant Orthopaedic surgeon

Martina Hansen's Hospital

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

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Knee Injury and Osteoarthritis Outcome Score

Time Frame: Preoperative until 2 years postoperatively

Patient relevant knee score. Validated score with 5 arms. 0-100, 100 is best.

Secondary Outcomes

  • UCLA Score(Preoperative until 2 years postoperatively)
  • Knee Injury and Osteoarthritis Outcome Score(10 years postoperatively)
  • Oxford Knee Score(10 years postoperatively)
  • Range of Motion(Preoperative until 2 years postoperatively)

Study Sites (3)

Loading locations...

Similar Trials