Correlation Study Between the Classification of Arthrogenic Motor Inhibition (AMI) and Clinical Assessment After ACL Rupture

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-44
SponsorGCS Ramsay Santé pour l'Enseignement et la Recherche

About this trial

The goal of this interventional study is to measure medial vastus inhibition and associate it with AMI classification in patients with ACL rupture. The main question it aims to answer is:

Is there a correlation between AMI classification and clinical assessment after ACL rupture ? Participants will undergo surface EMG and Myotonometry.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patient, male or female, aged ≥ 18 years and < 45 years

Patient with an ACL rupture confirmed by MRI

Patient with an ACL rupture ≤ 30 days old

French speaking patient who does not object to the use of his/her data

Disqualifiers

Patient with previous ipsi or contralateral knee injury/surgery

Patient with multi-ligament injury

Pregnant or breastfeeding woman

Trial design

Design model

Single group

Treatments tested in this trial

  • Clinical testing

    Other intervention

    Intervention includes : * Surface EMG to measure inhibition of the VM and the rectus femoris (RF) on the injured and non-injured sides during attempts at voluntary contractions of the knee extensor muscles. * Myotonometry to measure the stiffness of the semimembranosus and biceps femoris (long head) on the injured and non-injured sides under resting conditions

Treatment groups

90 Participants
are divided into 1 treatment group
Group A: AMI testing groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Muscle Surface EMG and AMI correlation

Electrical signal amplitude, expressed in mV, is evaluated at the level of the VM. This electrical signal amplitude is correlated with the level of muscle activation. It is measured with a surface EMG, which measures the activation of the VM during a voluntary attempt to contract the knee extensors. The ratio: Amplitude of the electrical signal from the injured side of the VM / Amplitude of the electrical signal from the non-injured side of the VM is used to determine the inhibition of the VM. AMI is assessed using the Sonnery-Cottet classification (Sonnery-Cottet et al, 2022)

Time frame
From enrollment to Day 30

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: