Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Investigating body composition's impact on stroke recovery

Official title: Prognostic Value for Predicting Functional Outcome Bioimpedancemetry and Temporal Muscle Measurement in Acute Stroke

Run by Centre Hospitalier Régional d'Orléans · NCT06589297 · Data updated 2026-11-12

This study tests how body composition affects recovery in stroke patients to see if it can help improve their rehabilitation plans.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment250 (estimated)
SponsorCentre Hospitalier Régional d'Orléans
Academic / other
Locations1 site (Orléans)
StatusRecruiting
StartedOctober 10, 2024
Main results expectedJune 2028
Study endsJune 2028
Registry record updatedFebruary 2, 2026
Trial IDNCT06589297 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adult stroke patients in the acute phase who can understand assessment guidelines.

Probably not a fit

Patients who are under legal protection, pregnant, or have certain medical devices like pacemakers may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study examines how body composition affects the recovery of patients who have experienced an acute stroke. It focuses on two bioimpedance parameters, skeletal mass index and phase angle, along with measurements of the temporal muscle's thickness and surface area. By analyzing these factors within the first 72 hours post-stroke, the study aims to predict functional outcomes at discharge and at a 6-month follow-up. The findings could help tailor rehabilitation strategies based on individual prognostic factors.

Why it matters

Potential benefit: If successful, this study could enhance recovery strategies for stroke patients by identifying key prognostic indicators.

How similar studies have gone: While the specific approach of using body composition metrics in acute stroke patients is novel, related studies have indicated that physiological factors can influence recovery outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* volunteer stroke patients in acute phase
* Age ≥ 18 years
* Having had a brain MRI
* Able to understand assessment guidelines
* Not having objected to participate in the study after being duly informed

Exclusion Criteria:

* Person under tutorship or curatorship
* Person under court protection
* Persons deprived of their liberty
* Pregnant or breastfeeding women
* Have a pacemaker or defibrillator

Where it's running

  • CHU d'ORLEANS
    Orléans, France
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.