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OpenTrials
Completed

NCT Number: NCT01765699

Predicting Poor Outcomes After Primary Knee Arthroplasty

Aim To identify through data analysis key patients, surgeon and operative dependent variables which will improve the performance of knee replacement for primary osteoarthritis

Research Question

1. Can the investigators identify association between outcomes and patients characteristics using existing (already collected) datasets 2. What are the characteristics of patients with poor outcome after knee replacement 3. What can be done to improve the outcome of patients at risk of poor results

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Key information

Conditions

Osteoarthritis, Knee Arthritis Joint Diseases Musculoskeletal Diseases Osteoarthritis Rheumatic Diseases

Sex eligibility

All sexes

Study type

Observational

About this study

This is a retrospective analysis of a prospectively collected single centre database.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Primary knee arthroplasty
  • Osteoarthritis

Exclusion criteria

  • No consent for joint registry data collection

Treatment and study plan

Primary knee arthroplasty

Device

Patients undergoing primary knee arthroplasty

Primary outcomes

  1. Change in PROMS

    Time frame: 1,2,3 and 5 Years post op

Sponsors and collaborators

Lead sponsor

Newcastle-upon-Tyne Hospitals NHS Trust

Other

Collaborators

  • DePuy Orthopaedics

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jan 10, 2013
Registry last updated
Oct 12, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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