Medico-Economic Evaluation of MRI Versus CT as Diagnostic Imaging Strategies in Patients With Suspected Ischemic Stroke: A Prospective, Multicenter, Randomized Controlled Two-Arm Parallel Trial: Transfusion Medicine - Blood Transfusion - Insurance News | InsuranceNewsNet

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August 3, 2026 Newswires
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Medico-Economic Evaluation of MRI Versus CT as Diagnostic Imaging Strategies in Patients With Suspected Ischemic Stroke: A Prospective, Multicenter, Randomized Controlled Two-Arm Parallel Trial: Transfusion Medicine – Blood Transfusion

Politics & Government Daily

2026 AUG 03 (NewsRx) -- By a News Reporter-Staff News Editor at Politics, Law & Government Daily -- Staff editors report on the newly launched clinical trial, NCT07719374, which has the following summary description: “Acute ischemic stroke (AIS) is a leading cause of death and long-term disability worldwide. In patients with suspected large vessel occlusion, rapid diagnosis and reperfusion therapy are critical, as treatment delays are associated with worse functional outcomes and increased mortality. Current French guidelines recommend brain magnetic resonance imaging (MRI) as the reference imaging modality because of its high diagnostic accuracy. However, MRI availability remains limited in many stroke centers, often resulting in delays in diagnosis and treatment. Conversely, computed tomography (CT) is more widely available and can substantially shorten time to reperfusion, although it may be less sensitive for early ischemic changes. The MAGRITTE study aims to determine whether an initial CT-based imaging strategy is more cost-effective than an MRI-based strategy for patients with suspected severe acute ischemic stroke within 6 hours of symptom onset. This is a prospective, multicenter, randomized controlled trial with two parallel groups enrolling 600 adult patients presenting with a high suspicion of acute ischemic stroke due to proximal large vessel occlusion (National Institutes of Health Stroke Scale \[NIHSS\] score ≥10). Participants will be randomized to undergo either CT with CT angiography or MRI with MR angiography as the first-line diagnostic imaging examination. Additional perfusion imaging may be performed at the investigator’s discretion. The primary objective is to compare the cost-utility of the two diagnostic strategies at 12 months, expressed as the incremental cost per quality-adjusted life year (QALY) gained, using EQ-5D-5L-derived utilities. Secondary objectives include lifetime cost-effectiveness modeling, 5-year budget impact analysis, comparison of functional outcomes, mortality, imaging-to-treatment and reperfusion times, symptomatic intracranial hemorrhage, diagnostic accuracy, management pathways, adverse events, radiation exposure, and healthcare costs. The study will provide evidence on whether a CT-first imaging strategy can improve the efficiency of acute stroke care while maintaining favorable clinical outcomes and reducing healthcare costs.”

As a matter of record, on July 23, 2026, NewsRx staff editors report that the available information provided by Fondation Ophtalmologique Adolphe de Rothschild on this trial include:

Tracking Information

Trial Identifier NCT07719374
First Submitted Date July 17, 2026
First Posted Date July 22, 2026
Results First Submitted Date Not Provided
Results First Posted Date Not Provided
Last Update Submitted Date July 17, 2026
Last Update Posted Date July 22, 2026
Primary Completion Date September 1, 2030
Start Date 2026-09-01
Current Primary Outcome Measures •Incremental cost per quality-adjusted life year (QALY) gained at 12 months [ Time Frame: 12 months after stroke onset ]
Current Secondary Outcome Measures Not Provided
Other Outcome Measures Not Provided
Change History Complete list of historical revisions of study NCT07719374

Descriptive Information

Brief Title Medico-Economic Evaluation of MRI Versus CT as Diagnostic Imaging Strategies in Patients With Suspected Ischemic Stroke: A Prospective, Multicenter, Randomized Controlled Two-Arm Parallel Trial.
Official Title Medico-Economic Evaluation of MRI Versus CT as Diagnostic Imaging Strategies in Patients With Suspected Ischemic Stroke: A Prospective, Multicenter, Randomized Controlled Two-Arm Parallel Trial.
Brief Summary Acute ischemic stroke (AIS) is a leading cause of death and long-term disability worldwide. In patients with suspected large vessel occlusion, rapid diagnosis and reperfusion therapy are critical, as treatment delays are associated with worse functional outcomes and increased mortality. Current French guidelines recommend brain magnetic resonance imaging (MRI) as the reference imaging modality because of its high diagnostic accuracy. However, MRI availability remains limited in many stroke centers, often resulting in delays in diagnosis and treatment. Conversely, computed tomography (CT) is more widely available and can substantially shorten time to reperfusion, although it may be less sensitive for early ischemic changes. The MAGRITTE study aims to determine whether an initial CT-based imaging strategy is more cost-effective than an MRI-based strategy for patients with suspected severe acute ischemic stroke within 6 hours of symptom onset. This is a prospective, multicenter, randomized controlled trial with two parallel groups enrolling 600 adult patients presenting with a high suspicion of acute ischemic stroke due to proximal large vessel occlusion (National Institutes of Health Stroke Scale \[NIHSS\] score ≥10). Participants will be randomized to undergo either CT with CT angiography or MRI with MR angiography as the first-line diagnostic imaging examination. Additional perfusion imaging may be performed at the investigator’s discretion. The primary objective is to compare the cost-utility of the two diagnostic strategies at 12 months, expressed as the incremental cost per quality-adjusted life year (QALY) gained, using EQ-5D-5L-derived utilities. Secondary objectives include lifetime cost-effectiveness modeling, 5-year budget impact analysis, comparison of functional outcomes, mortality, imaging-to-treatment and reperfusion times, symptomatic intracranial hemorrhage, diagnostic accuracy, management pathways, adverse events, radiation exposure, and healthcare costs. The study will provide evidence on whether a CT-first imaging strategy can improve the efficiency of acute stroke care while maintaining favorable clinical outcomes and reducing healthcare costs.
Detailed Description Not Provided
Study Type INTERVENTIONAL
Study Phase NA
Study Design Allocation: RANDOMIZED
Intervention Model: PARALLEL
Primary Purpose: DIAGNOSTIC
Masking: SINGLE
Condition Stroke
Intervention •DIAGNOSTIC_TEST: CT and CT angiography (CTA)
Participants randomized to this intervention undergo first-line non-contrast brain computed tomography (CT) and CT angiography (CTA) for the diagnosis of suspected acute ischemic stroke.
•DIAGNOSTIC_TEST: MRI and MR angiography (MRA)
Participants undergo first-line brain magnetic resonance imaging (MRI) and MR angiography (MRA) for the evaluation of suspected acute ischemic stroke.
Study Arms •ACTIVE_COMPARATOR: First-line brain MRI and MR angiography for suspected acute ischemic stroke.
Interventions:
⚬DIAGNOSTIC_TEST: MRI and MR angiography (MRA)
•EXPERIMENTAL: First-line non-contrast CT and CT angiography for suspected acute ischemic stro
Interventions:
⚬DIAGNOSTIC_TEST: CT and CT angiography (CTA)

Recruitment Information

Recruitment Status NOT_YET_RECRUITING
Enrollment 600
Completion Date 2030-09-01
Primary Completion Date September 1, 2030 (Final data collection date for primary outcome measure)
Eligibility Inclusion Criteria: * Age ≥18 years * Symptoms consistent with suspected acute ischemic stroke due to proximal large vessel occlusion * National Institutes of Health Stroke Scale (NIHSS) score ≥10 at admission * Symptom onset \<6 hours before randomization Exclusion Criteria: * Previous diagnostic brain imaging performed within the preceding 24 hours for the index stroke event * Contraindication to MRI (e.g., cardiac pacemaker, metallic implant or foreign body, surgical clips) or CT (e.g., pregnancy, severe renal impairment) * Contraindication to iodinated contrast agent (e.g., known severe allergy) * Not affiliated with the French national health insurance system * Not residing in France * Pregnant or breastfeeding * Adults under legal protection * Participation in another interventional clinical trial (RIPH1 or equivalent)
Sex/Gender Sexes Eligible for Study: ALL
Ages 18 years to
Accepts Healthy Volunteers f
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Not Provided
Removed Location Countries

Administrative Information

NCT Number NCT07719374
Other Study ID Numbers MMI-2025-5
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
Plan to Share Data Not Provided
Plan to Share Data (IPD) Description Not Provided
Collaborators Universite Paris Descartes- Laboratoire Interdisciplinaire de Recherche Appliquee en Economie-Gestion et Sante - LIRAES
Investigators Not Provided
Information Provided By Fondation Ophtalmologique Adolphe de Rothschild
Verification Date 2026-07

(Our reports deliver fact-based news of research and discoveries from around the world.)

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