- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02983929
Short-Term Follow-up Indicator for Total Knee Arthroplasty and Body Mass Index
Impact of Elevated Body Mass Index on Short-term Follow-up Indicators for Total Knee Arthroplasty : a Retrospective Study
The main purpose of this study is to determine the influence of obesity on the short term follow-up indicators of a polyvalent geriatric rehabilitation clinic after total knee arthroplasty. It is a retrospective, comparative study
The secondary purposes are to explore the links between length of stay and short-term follow-up indicators of a polyvalent geriatric rehabilitation clinic after total knee arthroplasty.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient admitted after total knee arthroplasty in Polyvalent Geriatric Rehabilitation Clinic during the january 2007/October 2016 period
Exclusion Criteria:
- Uncompleted case file or case file anterior to 2007 ;
- Inter-current orthopedic complication ;
- Evolutive or inter-current pathology written in the case-file (neurologic affection, etc...).
Study Plan
How is the study designed?
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
BMI <30 kg.m-2
Patients with a BMI inferior to the obesity limit defined by the World Health Organization.
|
All the included patients followed a rehabilitation program in the Polyvalent Geriatric Rehabilitation Clinic after total knee arthroplasty.
|
|
BMI >30 kg.m-2
Patients with a BMI superior to the obesity limit defined by the World Health Organization.
|
All the included patients followed a rehabilitation program in the Polyvalent Geriatric Rehabilitation Clinic after total knee arthroplasty.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Body Mass Index
Time Frame: 2 Month
|
2 Month
|
|
|
Range Of Motion of the Knee
Time Frame: 2 Month
|
The investigators will report the initial, final flexion and extension and calculate the total gain of flexion and extension of the knee for each participant.
|
2 Month
|
|
Age
Time Frame: 2 Month
|
2 Month
|
|
|
Mansat Score
Time Frame: 2 Month
|
This score is a composite score recommended by the French Authority of Health.
|
2 Month
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Length of stay
Time Frame: 2 month
|
The investigators will report the length of stay in the rehabilitation clinic for each participant.
|
2 month
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- MK1
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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