ClinicalTrials.Veeva

Menu

Evaluation of New Diagnostic Methods of Cardio-embolic Related (Atrial Fibrillation) Cerebral Infarction (IRMA2)

H

Hopital Foch

Status

Terminated

Conditions

Stroke

Treatments

Procedure: Abdominal scanner
Procedure: MRI

Study type

Interventional

Funder types

Other

Identifiers

NCT02948140
2016-A00020-51 (Other Identifier)
2016/02

Details and patient eligibility

About

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.

Enrollment

27 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

27 participants in 1 patient group

Stroke
Experimental group
Treatment:
Procedure: MRI
Procedure: Abdominal scanner

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems