- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04668677
Return to Work and Functional Results of French Soldiers After Anterior Cruciate Ligament Reconstruction
The return to work in the military population after surgical reconstruction of the anterior cruciate ligament (ACL) has been poorly investigated within the French armed forces. Only American studies are available and show that this surgery has a significant impact on the operational capacity of soldiers.
ACL rupture is extremely frequent in active populations. This pathology has already been extensively explored in at-risk populations, particularly in sports. Most studies show that the resumption of sport is greatly affected by this pathology.
Furthermore, an over-risk (10 times greater incidence of ACL rupture) in the military has been demonstrated.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Clamart, France, 92140
- Hôpital d'Instruction des Armées Percy
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Military personnel who underwent first-line ACL reconstruction surgery between January 2014 and May 2019
Exclusion Criteria:
- People who have had ACL reconstruction surgery after initial failure
- People with a multiligamentous knee condition
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Percentage of participants who regained their professional competence one year after anterior cruciate ligament (ACL) reconstruction surgery.
Time Frame: 1 year after anterior cruciate ligament (ACL) reconstruction surgery.
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1 year after anterior cruciate ligament (ACL) reconstruction surgery.
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020PPRC10
- 2020-A02234-35 (Other Identifier: IDRCB)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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