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Clinical Trials in France / NCT07199920
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Implementation of New Multimodal MRI Sequences by Fingerprint to Improve Ischemic Stroke Examination.

NCT07199920 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-10-01
Last updated
2025-09-30

Condition(s) studied

Stroke, Ischemic

Investigational drug(s) / intervention(s)

Achieva 3.0T dStream Philips

Achieva 3.0T dStream Philips: Classic and MRF sequences will be carried out on the clinical machine (Achieva 3.0T dStream Philips) of the IRMaGe platform (CHUGA, Université Grenoble Alpes, Inserm, CNRS).

Study summary

Currently, standard brain MRI takes 20 to 25 minutes, but in the case of ischemic stroke, every minute counts to limit the extension of the necrotic core, with the possibility of recanalizing the occluded artery (intravenous thrombolysis and/or mechanical thrombectomy).

The recent concept of MRI "Fingerprint" (Magnetic Resonance Fingerprinting, MRF) allows the production of a rapid single sequence and the extraction of numerous parameters.

Demonstrating the feasibility and interpretability of multimodal MRI images acquired in MRF would make it possible to consider implementing and, ultimately, replacing conventional sequences, with the aim of shortening acute stroke management times, increasing the number of sequences acquired within a short timeframe (by increasing informativeness), and thus improving patients\' short and long-term vital and functional prognosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \> 18 years * Subacute ischemic stroke patients (\< 15 days after onset) * Middle cerebral artery or anterior cerebral artery territory stroke * Modified Rankin Scale (mRS) = 0-4 Exclusion Criteria: \* MRI contraindications

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Chu Grenoble Alpes Grenoble France

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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 NCT07199920 on ClinicalTrials.gov ↗ ← All trials in France