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Recruiting NCT04781920

Follow-up of Anterior Cruciate Ligament Reconstruction

— Observational Anterior Cruciate Ligament Rupture

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: datas collection.
Who it may be relevant to
Registry conditions: Anterior Cruciate Ligament Rupture. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

Rupture of Anterior Cruciate Ligament (ACL) is a common pathology, but is subject to variability of associated lesions, surgical management and rehabilitation.

Detailed description

In this study, a collect data of patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction in order to evaluate the clinical, functional and morphological results of this intervention, in order to improve the management of the patient.

Interventions

  • Other datas collection
    data collection in history medical : operative report, clinical examination, questionnaires, imaging, isokinetic tests

Primary outcome measures

  • Analysis of Magnetic Resonance Imaging (MRI) results [Time frame: Pre-operative and Month: 12]
Secondary outcome measures (4)
  • Analysis of operative report results [Time frame: Month: 12]
  • Analysis of consultation report [Time frame: pre-operative and Months: 1,5 , 3, 6, 12]
  • Analysis of isokinetic tests [Time frame: Months: 9, 12]
  • Analysis of clinical surveys [Time frame: pre-operative and Months: 3, 6, 12]

Eligibility criteria

Inclusion criteria

  • Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction

Exclusion criteria

  • None

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

France · 1 center
  • Chu Saint-Etienne — Saint-Etienne

Identifiers

NCT: NCT04781920 · IRBN162021/CHUSTE

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗