Body Composition and Acute Stroke

NCT06589297 · tracked via the Priya Life Science France tracker

Sponsor

Centre Hospitalier Régional d'Orléans

Phase

Not applicable

Started

2024-10-10

Last updated

2026-02-02

Condition(s) studied

Acute Stroke

Investigational drug(s) / intervention(s)

Modified Rankin scale

Modified Rankin scale: Acute stroke patients will undergo modified rankin scale

Study summary

Body composition appears to be a prognostic factor for the severity and functional outcome of stroke patients. In this study the prognostic value of two bioimpedance parameters will be studied (skeletal mass index and phase angle) and two temporal muscle measurements (thickness and surface area) to predict the functional outcome of patients at discharge and at 6 months

Eligibility

Sex

ALL

Min age

18 Years

Max age

—

Healthy volunteers

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

Primary outcome measure(s)

phase angle — 72 hours after stroke
thickness of temporal muscle — 72 hours after stroke
surface area of temporal muscle — 72 hours after stroke

Trial sites (1)

Facility	City	Region	Status
CHU d'ORLEANS	Orléans	France	Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06589297 on ClinicalTrials.gov ↗ ← All trials in France