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Short-Term Follow-up Indicator for Total Knee Arthroplasty and Body Mass Index

NCT ID: NCT02983929

Last Updated: 2016-12-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

244 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-01-31

Study Completion Date

2016-11-30

Brief Summary

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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.

Detailed Description

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Conditions

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Total Knee Arthroplasty Body Mass Index Rehabilitation

Study Groups

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BMI <30 kg.m-2

Patients with a BMI inferior to the obesity limit defined by the World Health Organization.

Rehabilitation after total knee arthroplasty

Intervention Type PROCEDURE

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.

Rehabilitation after total knee arthroplasty

Intervention Type PROCEDURE

All the included patients followed a rehabilitation program in the Polyvalent Geriatric Rehabilitation Clinic after total knee arthroplasty.

Interventions

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Rehabilitation after total knee arthroplasty

All the included patients followed a rehabilitation program in the Polyvalent Geriatric Rehabilitation Clinic after total knee arthroplasty.

Intervention Type PROCEDURE

Eligibility Criteria

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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...).
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Durécu Lavoisier

OTHER

Sponsor Role lead

Responsible Party

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Timothée Gillot

Physical therapist, Msc.

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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MK1

Identifier Type: -

Identifier Source: org_study_id