Interest of the T2 * Sequence in MRI for the Diagnosis of Migraine Aura in the Acute Phase.
NCT ID: NCT03689361
Last Updated: 2021-02-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
60 participants
INTERVENTIONAL
2018-12-22
2020-12-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
DOUBLE
Study Groups
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with migraine aura.
patient with migraine aura detected by MRI, then MRI control 3 month after
MRI
Routine MRI with all the sequences performed for the management of acute neurological deficit in the Toulouse Neuro Vascular Unit (diffusion, FLAIR, T2 \*, vascular sequences (AngioRM and TOF) and perfusion).
MRI control
MRI with all the sequences performed for the management of acute neurological deficit in the Toulouse Neuro Vascular Unit (diffusion, FLAIR, T2 \*, vascular sequences (AngioRM and TOF) and perfusion)
without migraine aura
patient without migraine aura detected by MRI, then telephone consultation 3 month after
telephone consultation
telephone consultation
Interventions
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MRI
Routine MRI with all the sequences performed for the management of acute neurological deficit in the Toulouse Neuro Vascular Unit (diffusion, FLAIR, T2 \*, vascular sequences (AngioRM and TOF) and perfusion).
MRI control
MRI with all the sequences performed for the management of acute neurological deficit in the Toulouse Neuro Vascular Unit (diffusion, FLAIR, T2 \*, vascular sequences (AngioRM and TOF) and perfusion)
telephone consultation
telephone consultation
Eligibility Criteria
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Inclusion Criteria
* Admitted to the Neuro-Vascular Intensive Care Unit for Acute Focused Neurological Symptoms and MRI
* less than 4 hours 30 minutes after onset of symptoms if symptoms persist during admission
* less than two hours after the disappearance of symptoms if the patient arrives asymptomatic
* Affiliated to a social protection scheme.
* Having given their informed consent
Exclusion Criteria
* Presence of recent explanatory abnormalities on the MRI to make a diagnosis compatible with the initial neurological symptomatology (visible stroke in diffusion, cerebral hemorrhage, tumor, arteriovenous malformations).
* Potential strong cause of stroke known or discovered at the arrival of the patient, in particular stenosis of a cervical or intracranial artery upstream of the cerebral zone may correspond to the symptoms and emboligenic heart disease type atrial fibrillation.
* Pregnant women - Patients with a contraindication for MRI.
* Patients benefiting from a system of legal protection (tutelage,
18 Years
55 Years
ALL
No
Sponsors
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University Hospital, Toulouse
OTHER
Responsible Party
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Principal Investigators
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Alain Viguier, PH
Role: PRINCIPAL_INVESTIGATOR
Uuniversity Hospital Toulouse
Locations
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HĂ´pital Pierre Paul Riquet - CHU de Toulouse
Toulouse, , France
Countries
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Other Identifiers
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2017-004091-60
Identifier Type: EUDRACT_NUMBER
Identifier Source: secondary_id
RC31/16/8249
Identifier Type: -
Identifier Source: org_study_id
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