Follow-up of Anterior Cruciate Ligament Reconstruction

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Saint Etienne

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction

Disqualifiers

None

Trial population

Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction will be included.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • datas collection

    Other intervention

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

Treatment groups

200 Participants
are divided into 1 treatment group
Group A: Patients having undergone an Anterior Cruciate Ligament (ACL) reconstruction1 intervention

Trial outcomes

Primary outcomes

1

Analysis of Magnetic Resonance Imaging (MRI) results

Collected in medical records

Time frame
Pre-operative and Month: 12

Secondary outcomes

1

Analysis of operative report results

Collected in medical records

Time frame
Month: 12
2

Analysis of consultation report

Collected in medical records

Time frame
pre-operative and Months: 1,5 , 3, 6, 12
3

Analysis of isokinetic tests

Collected in medical records

Time frame
Months: 9, 12
4

Analysis of clinical surveys

Collected in medical records

Time frame
pre-operative and Months: 3, 6, 12

Other outcomes

Sponsors and contacts

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