Skip to main content
OpenTrials
Recruiting

NCT Number: NCT04781920

Follow-up of Anterior Cruciate Ligament Reconstruction

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

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Anterior Cruciate Ligament Rupture Anterior Cruciate Ligament Injuries Knee Injuries Leg Injuries Wounds and Injuries

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Chu Saint-Etienne

Saint-Etienne, France

Location status: Recruiting

Location contact

Alban STORDEUR, resident

SUB_INVESTIGATOR

Rémi PHILIPPOT, MD PhD

SUB_INVESTIGATOR

Thomas NERI, MD

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • None

Treatment and study plan

datas collection

Other

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

Primary outcomes

  1. Analysis of Magnetic Resonance Imaging (MRI) results

    Time frame: Pre-operative and Month: 12

    Collected in medical records

Secondary outcomes

  1. Analysis of operative report results

    Time frame: Month: 12

    Collected in medical records

  2. Analysis of consultation report

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

    Collected in medical records

  3. Analysis of isokinetic tests

    Time frame: Months: 9, 12

    Collected in medical records

  4. Analysis of clinical surveys

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

    Collected in medical records

Study contacts

Contact information is provided by the study sponsor or research team.

Alban STORDEUR, resident

CONTACT

[email protected]

(0)477127849 ext. +33

Thomas NERI, MD

CONTACT

[email protected]

(0)477127849 ext. +33

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire de Saint Etienne

Other

Registry information

Important dates

Study start
2021
Primary completion
2025
Study completion
2027
First posted
Mar 4, 2021
Registry last updated
Aug 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.