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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05521555
Other study ID # 2022-A00947-36
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 20, 2022
Est. completion date September 20, 2022

Study information

Verified date August 2022
Source Central Hospital, Nancy, France
Contact Didier Mainard, PHD
Phone 03 83 85 17 82
Email didier.mainard@univ-lorraine.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study takes its base in the augmenting number of primary total knee arthroplasty in the world whom quality and survey had permit to widen their indications to younger patients who are in the age of professional activity. This work will focus on young patients under 55 who had had primary total knee arthroplasty, retrospectively, over the past 10 years, to determine the factors influencing early or late return to work, depending of socio economics factors. This will optimize the information for the patient, and prepare him if necessary for a long work stop, and possibly obtain a better satisfaction for him.


Description:

The primary aim of this study is to determine the rate of young patients returning to work after a primary total knee arthroplasty and the mean delay, and to compare it to other studies. The mean delay of return to work in the literature is between 8 to 12 weeks, with up to 98% of patients returning to work. The investigators will next determine which category of patients could have a late return to work superior to 6 months, and also if the surgery could give back a professional activity to patients who were in a long work stoppage.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date September 20, 2022
Est. primary completion date September 10, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - first intention total knee arthroplasty - Age at the time of surgery under 55 Exclusion Criteria: - Not in capacity of completing a questionnaire - revision of total knee arthroplasty

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Total knee arthroplasty
First intention total knee arthroplasty

Locations

Country Name City State
France CHRU Nancy, Hopital central Nancy Meurthe Et Moselle

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Return to work in weeks Duration between surgery and return to work 2 years
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