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Disability and Self-rated Health Following Primary Knee Replacement

This study is ongoing, but not recruiting participants.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01236729
First Posted: November 9, 2010
Last Update Posted: August 8, 2017
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborator:
University of Tampere
Information provided by (Responsible Party):
Esa Jamsen, Coxa, Hospital for Joint Replacement
December 22, 2009
November 9, 2010
August 8, 2017
December 2009
June 2013   (Final data collection date for primary outcome measure)
Disability in activities of daily living [ Time Frame: Baseline (recruitment) and at 12 months ]
Same as current
Complete list of historical versions of study NCT01236729 on ClinicalTrials.gov Archive Site
  • Overall self-rated health [ Time Frame: Baseline (recruitment) and at 12 months ]
  • Health-related quality of life (WOMAC) [ Time Frame: Baseline and 12 months postoperatively ]
    For patients recruited in 2011-2012.
Overall self-rated health [ Time Frame: Baseline (recruitment) and at 12 months ]
Not Provided
Not Provided
 
Disability and Self-rated Health Following Primary Knee Replacement
The Effects of Primary Knee Replacement for Osteoarthritis on Disability in Activities of Daily Living and Self-rated Health in Older People
Knee replacement is an effective treatment in late-stage osteoarthritis. It reduces pain and improves quality of life. There is, however, limited data concerning its results in older people and on its effect on how patients survive in regular activities of daily living (ADL), such as bathing and shopping. In this study, the results of knee replacement are evaluated from the point of view of disability in everyday activities and self-rated health. Moreover, association with ADL performance and clinical knee scores and severity of osteoarthritis are assessed.
This is a cross-sectional study with a 12 month follow-up for recruited patients. Most data are gathered by a postal questionnaire.
Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Not Provided
Non-Probability Sample
Patients refererred to or operated on with primary knee replacement in a population-based tertiary care hospital
  • Osteoarthritis
  • Knee Replacement
Not Provided
Knee replacement recipients
Patients (aged 75 years or over) with late-stage arthritis who have undergone or are undergoing primary knee replacement

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
460
December 2017
June 2013   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • age 75 years or more at the time of operation
  • diagnosis of knee osteoarthritis
  • scheduled for or operated on with primary knee replacement

Exclusion Criteria:

  • died during the follow-up
  • inflammatory arthritides
Sexes Eligible for Study: All
75 Years and older   (Senior)
No
Contact information is only displayed when the study is recruiting subjects
Finland
 
 
NCT01236729
KL122009
No
Not Provided
Not Provided
Esa Jamsen, Coxa, Hospital for Joint Replacement
Coxa, Hospital for Joint Replacement
University of Tampere
Study Director: Esa Jämsen, MD, PhD Coxa, Hospital for Joint Replacement
Coxa, Hospital for Joint Replacement
August 2017