Skip to content

Follow-up of Anterior Cruciate Ligament Reconstruction

Follow-up of Anterior Cruciate Ligament Reconstruction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04781920
Enrollment
200
Registered
2021-03-04
Start date
2021-03-01
Completion date
2027-09-30
Last updated
2024-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Cruciate Ligament Rupture

Keywords

Anterior Cruciate Ligament, reconstruction, Operative report, Consultation report, Isokinetic tests, Clinical surveys

Brief summary

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

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

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Analysis of Magnetic Resonance Imaging (MRI) resultsPre-operative and Month: 12Collected in medical records

Secondary

MeasureTime frameDescription
Analysis of operative report resultsMonth: 12Collected in medical records
Analysis of consultation reportpre-operative and Months: 1,5 , 3, 6, 12Collected in medical records
Analysis of isokinetic testsMonths: 9, 12Collected in medical records
Analysis of clinical surveyspre-operative and Months: 3, 6, 12Collected in medical records

Countries

France

Contacts

Primary ContactThomas NERI, MD
thomas.neri@chu-st-etienne.fr(0)477127849
Backup ContactAlban STORDEUR, resident
alban.stordeur@gmail.com(0)477127849

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026