Neuromuscular Profiles After Anterior Cruciate Ligament Reconstruction
Exploratory Study of Neuromuscular Profiles After Anterior Cruciate Ligament Reconstruction in Clinical Conditions: Combined Analysis of Isokinetic Strength and Surface Electromyography
- Anterior Cruciate Ligament Injury
At a glance
- Phase
- Phase not stated
- Study type
- Observational
- Sponsor
- Hopitaux de Saint-Maurice
- Enrolment target
- 30
- Started
- 21 August 2026
- Main results due
- 1 December 2026
- Study sites
- 1
- Registry updated
- 29 September 2026
Can you take part?
- Aged 18 years and over.
- Open to any sex.
- You need the condition being studied — healthy volunteers are not accepted.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility criteria
Inclusion Criteria: * Anterior cruciate ligament (ACL) reconstruction. * Postoperative period between 4 and 12 months. * Age 18 years or older. * Affiliation with or beneficiary of a social security scheme. * Ability to understand the study information and to express non-opposition to participation. Exclusion Criteria: * Persons under guardianship, curatorship, or another legal protection measure. * Any condition preventing safe performance of isokinetic testing, including significant pain, significant joint effusion, substantial limitation of joint range of motion, clinical knee instability, or an ongoing postoperative complication. * Opposition to participation in the study.
What this study is about
In the sponsor’s own words, from the registry.
The NEURO-ACL-ISOEMG study is an observational, cross-sectional, exploratory study conducted in patients between 4 and 12 months after anterior cruciate ligament (ACL) reconstruction.
The primary objective is to describe the joint distribution of isokinetic muscle strength and surface electromyographic (sEMG) activation parameters of the quadriceps and hamstrings in order to explore different neuromuscular profiles under clinical conditions.
The study combines data from the routine functional assessment, including isokinetic strength measurements and a single-leg hop test, with surface electromyography and patient-reported questionnaires assessing knee self-efficacy, kinesiophobia, symptoms, and knee function.
Study sites(1)
Hôpitaux Paris Est Val-de-Marne - Service de rééducation orthopédique et traumatologie
Saint-Maurice, Demande, France
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07792863. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
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