Interest of Occlusion of Permeable Foramen Ovale After a Cryptogenic Cerebrovascular Accident (CVA) (FOPasa)

N

Nantes University Hospital (NUH)

Status

Completed

Conditions

Cerebrovascular Accident
Permeable Foramen Ovale

Treatments

Other: Data collection

Study type

Observational

Funder types

Other

Identifiers

NCT00872443
BRD 08/8-J

Details and patient eligibility

About

Facing the lack of recommandations of Neurology and cardiology societies, the investigators decided in 2002 some Good Medical Practices to define a specific and precise population for whom the closure of permeable oval formaen after a first CVA seem to be necessary. Current survey of these patients after implantation of a prothesis in interauricular septum is defined by a consultation at 1, 3 and 6 months after surgery for a clinical exam and an echocardiography. One year after implantation, the investigators systematically realized a control by MRI associated to a contrast echography. In the aim of evaluating the investigators' medical practice, the investigators decided to do an observational study which will permit us to judge of the interest or lack of interest of our "Good medical practice" before the publication of prospective and randomised clinical studies.

Enrollment

72 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • less than 55 years old
  • occlusion of FOP after cryptogenic CVA

Exclusion criteria

  • characterized thromboembolic event
  • patients who have a surgery after transitory ischemic accident

Trial design

72 participants in 1 patient group

FOP
Description:
Patients who already have an occlusion of POF secondary to a cryptogenic CVA and younger than 55 years old and without characterized thromboembolic events.
Treatment:
Other: Data collection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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