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

This study is ongoing, but not recruiting participants.
Sponsor:
Collaborator:
South-Eastern Norway Regional Health Authority
Information provided by:
Martina Hansen's Hospital
ClinicalTrials.gov Identifier:
NCT01032538
First received: December 14, 2009
Last updated: NA
Last verified: December 2009
History: No changes posted
  Purpose

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.


Condition
Osteoarthritis

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official 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

Resource links provided by NLM:

U.S. FDA Resources

Further study details as provided by Martina Hansen's Hospital:

Primary Outcome Measures:
  • Knee injury and Osteoarthritis Outcome Score [ Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Range of Motion [ Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively ] [ Designated as safety issue: No ]
  • Oxford knee score [ Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively ] [ Designated as safety issue: No ]
  • UCLA score [ Time Frame: Preoperative and 6 weeks, 3 months, 6 months, 1 year, and 2 years postoperatively ] [ Designated as safety issue: No ]
  • Knee injury and Osteoarthritis Outcome Score [ Time Frame: 6 years and 10 years postoperatively ] [ Designated as safety issue: No ]

Enrollment: 100
Study Start Date: November 2003
Estimated Study Completion Date: February 2017
Primary Completion Date: February 2009 (Final data collection date for primary outcome measure)
Groups/Cohorts
Patients with knee osteoarthritis

  Eligibility

Ages Eligible for Study:   50 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population

Consecutive patients operated with total knee arthroplasty at Martina Hansens Hospital, Akershus University Hospital and Baerum hospital

Criteria

Inclusion Criteria:

  • patients with medial knee osteoarthritis
  • admitted for unicondylar knee replacement
  • no rheumatoid arthritis
  • no previous knee infection
  • age 50-80 years
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01032538

Locations
Norway
Bærum Sykehus
Bærum, Akershus, Norway, 1309
Akershus University Hospital
Lørenskog, Akershus, Norway, 1478
Martina Hansens Hospital
Bærum, Norway, 1306
Sponsors and Collaborators
Martina Hansen's Hospital
South-Eastern Norway Regional Health Authority
Investigators
Principal Investigator: Tor Kjetil Nerhus, MD Martina Hansens Hospital
  More Information

No publications provided

Responsible Party: Tor Kjetil Nerhus/ Consultant orthopaedic surgeon, Martina Hansens Hospital
ClinicalTrials.gov Identifier: NCT01032538     History of Changes
Other Study ID Numbers: TKN-002, 19441 (NSD)
Study First Received: December 14, 2009
Last Updated: December 14, 2009
Health Authority: Norway: Norwegian Social Science Data Services

Keywords provided by Martina Hansen's Hospital:
Unicondylar Knee Replacement

Additional relevant MeSH terms:
Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases

ClinicalTrials.gov processed this record on May 23, 2013