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

Implementation of New Multimodal MRI Sequences by Fingerprint to Improve Ischemic Stroke Examination, a Pilot Study and Proof of Concept

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07199920
Acronym
INDEX
Enrollment
10
Registered
2025-09-30
Start date
2025-10-01
Completion date
2027-01-01
Last updated
2025-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke, Ischemic

Keywords

MRF (Magnetic Resonance Fingerprinting), stroke, MRI

Brief 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.

Interventions

DEVICEAchieva 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).

Sponsors

Grenoble Institut des Neurosciences
CollaboratorOTHER
University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SEQUENTIAL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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

Design outcomes

Primary

MeasureTime frameDescription
Success rate and interpretability of images acquired in MRFFrom enrollment to the end of the MRI examAssessment of the success rate and interpretability (subjective evaluation with Likert scales of very satisfactory, satisfactory, insufficient, or unacceptable)

Secondary

MeasureTime frameDescription
Characterize and extract the physical parameters of the signal acquired with MRF.From enrollment to the end of the MRI examComparison of MRF imaging metrics: signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR), using mean values per ROI (region of interest). Segmentation and comparison of lesions, with calculation of the Dice similarity coefficient and/or SSIM (Structural SIMilarity). Visualization and description of artifacts encountered during acquisition (e.g., motion). Quantification of delays: Acquisition time: retrieval of raw data directly from MRI consoles. Reconstruction time: measurement of computation times. Extraction of information on cerebral microvas

Countries

France

Contacts

Primary ContactZaza Putkaradze, Dr
zputkaradze@chu-grenoble.fr0476767842

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026