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Implementation of New Multimodal MRI Sequences by Fingerprint to Improve Ischemic Stroke Examination. (INDEX)

Grenoble Alpes University Hospital Center (CHU) logo

Grenoble Alpes University Hospital Center (CHU)

Status

Not yet enrolling

Conditions

Stroke, Ischemic

Treatments

Device: Achieva 3.0T dStream Philips

Study type

Interventional

Funder types

Other

Identifiers

NCT07199920
38RC23.0410

Details and patient eligibility

About

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.

Enrollment

10 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Sequential Assignment

Masking

None (Open label)

10 participants in 1 patient group

Experimental
Experimental group
Description:
Every patient will perform classic brain MRI with additional MRF sequences.
Treatment:
Device: Achieva 3.0T dStream Philips

Trial contacts and locations

1

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Central trial contact

Zaza Putkaradze, Dr

Data sourced from clinicaltrials.gov

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