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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03689361
Other study ID # RC31/16/8249
Secondary ID 2017-004091-60
Status Completed
Phase Phase 4
First received
Last updated
Start date December 22, 2018
Est. completion date December 11, 2020

Study information

Verified date February 2021
Source University Hospital, Toulouse
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

investigators hypothesize that T2 * vein abnormalities are frequent and are specific to the migraine aura.


Description:

The diagnosis of migraine aura is now based solely on clinical criteria and the assertion of the diagnosis on these clinical criteria alone proves difficult in the acute phase. Added to this difficulty, the symptomatology of a migraine aura can sometimes be similar to that of a stroke, so a diagnosis can be poorly established, resulting in poor patient care. The possibility of making the positive diagnosis of migraine aura on a routine MRI sequence, T2 *, would be an important advance for the management of these patients


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 11, 2020
Est. primary completion date October 11, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - Patients aged 18 to 55 years - 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: - Patients with neurological signs pointing to vertebrobasilar localization (vertigo, diplopia) or with a disorder of consciousness - 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,

Study Design


Related Conditions & MeSH terms


Intervention

Combination Product:
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).
Diagnostic Test:
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)
Other:
telephone consultation
telephone consultation

Locations

Country Name City State
France Hôpital Pierre Paul Riquet - CHU de Toulouse Toulouse

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Toulouse

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary frequency of the presence of visible brain vein abnormalities visible brain vein abnormalities on T2 * sequences MRI , Day 0
Secondary perfusion parameters in MRI , Overall visual assessment: presence or absence of hypoperfusion (presence or not in each anterior, middle and posterior territory) each lobe: Frontal, Temporal, Parietal, Occipital) Day 0
Secondary asymmetry of visualization of the 3 intracranial arteries in MRI in MRI TOF Day 0