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Clinical Trials/NCT02369328
NCT02369328
Unknown
Not Applicable

Multimodal MRI Study of Ischemic Stroke

Assistance Publique Hopitaux De Marseille1 site in 1 country60 target enrollmentFebruary 2015
ConditionsSTROKE

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
STROKE
Sponsor
Assistance Publique Hopitaux De Marseille
Enrollment
60
Locations
1
Primary Endpoint
The time of stroke onset
Last Updated
9 years ago

Overview

Brief Summary

Stroke is the second most frequent causes of mortality in the word after cardiovascular disease and the most frequent cause of disability. The majority of strokes are ischemic (87%). Ischemic stroke may benefit from efficient therapy if the delay from stroke onset not exceeds 4H30 (intra-venous thrombolysis). In case of irreversible cerebral lesion, the long term functional recovery is largely dependent from the ability of the brain to reorganize. Conventional magnetic resonance imaging represents the most sensitive tool to diagnose stroke at the acute phase. However, up to now, no imaging tool is available to determine the time of stroke onset. Moreover, no imaging tool is available to precisely quantify the functional and structural plasticity mechanisms occurring after stroke. The main objective of the present study is to test the accuracy of sodium MRI to determine the time of stroke onset. The secondary objectives of the study are to determine the ability of non-conventional MRI techniques to quantify the degree of tissue damage and brain reorganization after stroke. Thirty patients will be included during the first 24 hours after stroke onset. Multimodal MRI (including perfusion MRI, sodium MRI, resting-state functional MRI, high resolution anatomical MRI) and clinical evaluation will be carried on at the inclusion, after 24 hours, at 3 months and at 12 months.

Registry
clinicaltrials.gov
Start Date
February 2015
End Date
June 2018
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient having presented a cerebral infarct beforehand confirmed by the brain imaging
  • Patient having presented a cerebral infarct the hour of the beginning of which is known with certainty and dating less than 24 hours
  • Patient having presented a cerebral infarct the area(extent) of which is superior to 1,5 ml

Exclusion Criteria

  • Patients presenting the usual contraindications to the MRI (pacemaker, agitation, metallic brightness, claustrophobia etc.)
  • Patients presenting a risk of not compliance to the examination: disorders(confusions) of the elementary understanding, the confusion, the involuntary movements, the bad tolerance of the prolonged dorsal decubitus

Outcomes

Primary Outcomes

The time of stroke onset

Time Frame: 3 years

The main objective of the present study is to test the accuracy of sodium MRI to determine the time of stroke onset

Secondary Outcomes

  • The degree of tissue damage and brain reorganization after stroke(3 years)

Study Sites (1)

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