Predicting Poor Outcomes After Primary Knee Arthroplasty
1 other identifier
observational
1,300
0 countries
N/A
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2012
Shorter than P25 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
February 1, 2012
CompletedFirst Submitted
Initial submission to the registry
December 31, 2012
CompletedFirst Posted
Study publicly available on registry
January 10, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2013
CompletedOctober 12, 2015
October 1, 2015
1 year
December 31, 2012
October 7, 2015
Conditions
Outcome Measures
Primary Outcomes (1)
Change in PROMS
1,2,3 and 5 Years post op
Study Arms (1)
Primary knee arthroplasty
Patients with osteoarthritis of the knee undergoing primary knee arthroplasty
Interventions
Patients undergoing primary knee arthroplasty
Eligibility Criteria
Patients who have undergone primary knee arthroplasty in our centre.
You may qualify if:
- Primary knee arthroplasty
- Osteoarthritis
You may not qualify if:
- No consent for joint registry data collection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Newcastle-upon-Tyne Hospitals NHS Trustlead
- DePuy Orthopaedicscollaborator
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Craig Gerrand
Consultant Orthopaedic Surgeon
- STUDY DIRECTOR
David Deehan
Consultant Orthopaedic Surgeon
Study Design
- Study Type
- observational
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 31, 2012
First Posted
January 10, 2013
Study Start
February 1, 2012
Primary Completion
February 1, 2013
Study Completion
February 1, 2013
Last Updated
October 12, 2015
Record last verified: 2015-10