Study Results
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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RECRUITING
200 participants
OBSERVATIONAL
2021-03-01
2027-09-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction
Patients having undergone an ACL reconstruction will be included.
datas collection
data collection in history medical : operative report, clinical examination, questionnaires, imaging, isokinetic tests
Interventions
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datas collection
data collection in history medical : operative report, clinical examination, questionnaires, imaging, isokinetic tests
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Saint Etienne
OTHER
Responsible Party
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Principal Investigators
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Thomas NERI, MD
Role: PRINCIPAL_INVESTIGATOR
CHU SAINT-ETIENNE
Locations
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Chu Saint-Etienne
Saint-Etienne, , France
Countries
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Central Contacts
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Other Identifiers
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IRBN162021/CHUSTE
Identifier Type: -
Identifier Source: org_study_id
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