Evaluation of New Diagnostic Methods of Cardio-embolic Related (Atrial Fibrillation) Cerebral Infarction

Study Results

Results pending

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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Recruitment Status

TERMINATED

Clinical Phase

NA

Total Enrollment

27 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-06-13

Study Completion Date

2020-12-31

Brief Summary

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The aim of the study is to estimate the contribution of abdominal imaging by magnetic resonance Imaging (MRI) and abdominal scanner in the detection of subdiaphragmatic infarction associated to the atrial fibrillation in the cerebral infarction.

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Detailed Description

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Conditions

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Stroke

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Stroke

Group Type EXPERIMENTAL

MRI

Intervention Type PROCEDURE

Abdominal scanner

Intervention Type PROCEDURE

Interventions

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MRI

Intervention Type PROCEDURE

Abdominal scanner

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient over 18
* Patient having a CHADS-VAsc Score ≥ 2;
* Patient hospitalized for a secondary established ischemic accident in an atrial fibrillation not anticoagulated (INR\<2 and/or receiving antiplatelet (aspirin, clopidogrel)) for less than 14 days;
* Patient affiliated to a national insurance scheme or beneficiary
* Patient having given a written consent

Exclusion Criteria

* Patient presenting cognitive disorders incompatible with the planned examinations (MRI / SCANNER).
* Pacemaker or implantable defibrillator, or other contraindication in the MRI (metallic eye brightness, intra cerebral clip).
* Contraindication in injected scanner.
* Current pregnancy

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No