International PFO Consortium

Last updated: December 11, 2017
Sponsor: University Hospital Inselspital, Berne
Overall Status: Active - Recruiting

Phase

N/A

Condition

Stroke

Circulation Disorders

Cerebral Ischemia

Treatment

N/A

Clinical Study ID

NCT00859885
117/08
  • Ages > 18
  • All Genders

Study Summary

The prevalence of patent foramen ovale (PFO) is about 25% in the general population and approximately 40% in patients who have ischemic stroke of unknown cause (cryptogenic stroke). Given the large number of asymptomatic patients, no primary prevention is currently recommended. On the contrary, secondary prevention is very important. Prospective studies have shown that antithrombotic treatment (ATT) with aspirin or warfarin appears to negate the risk of recurrent stroke associated with a PFO. Patients with spontaneous or large right-to-left shunts (RLS), those with a coinciding atrial septal aneurysm (ASA) or multiple ischemic events prior to the PFO diagnosis may still be at increased risk of stroke recurrence despite ATT. Percutaneous device closure (PDC) is a challenging alternative to ATT. Several studies reported 0% to 3.4% annual recurrence rates of stroke or TIA in patients treated by PDC. To date, there is no data from randomized controlled trials (RCT) comparing the risk of stroke recurrence after PDC with that under ATT only. The results from ongoing RCTs are not to be awaited in the near future, mainly due to low enrolment and event rates. Alternative data-gathering strategies such as multicenter registries are needed to overcome the low recruitment rates. The aim of the present study is to compare the risk of recurrent stroke and TIA in patients with PFO and otherwise unexplained stroke who undergo PDC or receive ATT.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age > 18 years

  • Diagnosis of PFO established by transesophageal echocardiography (TEE)

  • Ischemic stroke or transient ischemic attack within the previous 6 months

Exclusion Criteria

  • Non-vascular origin of the neurological symptoms after brain imaging (CT scan or MRI)

  • Comorbid condition that would interfere with the study

  • Pregnancy

  • History of intracranial bleeding, confirmed arterio-venous malformation, aneurysm or uncontrolled coagulopathy

  • Contraindications for TEE, echocardiographic or iodine contrast media

Study Design

Total Participants: 1500
Study Start date:
September 08, 2008
Estimated Completion Date:
December 31, 2021

Study Description

Background

The prevalence of patent foramen ovale (PFO) is about 25% in the general population and approximately 40% in patients who have ischemic stroke of unknown cause (cryptogenic stroke). Given the large number of asymptomatic patients, no primary prevention is currently recommended. On the contrary, secondary prevention is very important. Prospective studies have shown that antithrombotic treatment (ATT) with aspirin or warfarin appears to negate the risk of recurrent stroke associated with a PFO. Patients with spontaneous or large right-to-left shunts (RLS), those with a coinciding atrial septal aneurysm (ASA) or multiple ischemic events prior to the PFO diagnosis may still be at increased risk of stroke recurrence despite ATT. Percutaneous device closure (PDC) is a challenging alternative to ATT. Several studies reported 0% to 3.4% annual recurrence rates of stroke or TIA in patients treated by PDC. To date, there is no data from randomized controlled trials (RCT) comparing the risk of stroke recurrence after PDC with that under ATT only. The results from ongoing RCTs are not to be awaited in the near future, mainly due to low enrolment and event rates. Even if RCTs are completed successfully, statistical differences may remain undetected with the planned sample sizes. Alternative data-gathering strategies such as multicenter registries are needed to overcome the low recruitment rates.

Objective

  1. To compare the risk of recurrent stroke and TIA in patients aged ≤ 55 years with PFO and otherwise unexplained stroke who undergo PDC or receive ATT only; 2) To assess the etiological role of PFO for stroke/TIA in patients aged > 55 years; 3) To assess the risk of recurrent stroke/TIA in "high-risk" PFO patients (i.e. those with spontaneous (at rest) or large RLS, coinciding ASA, or multiple previous cerebrovascular events).

Methods

Multicenter prospective non-randomized study with scheduled 3-years follow-up of patients with PFO and ischemic stroke or TIA. Participating centers: Swiss University Hospitals of Basel, Bern, Geneva, Lausanne and Zurich, the Cantonal Hospital of Aarau, the Triemli Hospital, the Alfried-Krupp Krankenhaus of Essen, the University Hospital of Essen, the Klinikum Worms gGmbH, Tufts Medical Center, Baystate Medical Center, the East Medical Center Tyler, and the University Hospital of Leuven.

Connect with a study center

  • University Hospital Gent

    Gent, 9000
    Belgium

    Active - Recruiting

  • Leuven University Hospital

    Leuven, 3000
    Belgium

    Active - Recruiting

  • Alfried Krupp Hospital

    Essen, 45117
    Germany

    Active - Recruiting

  • Essen University Hospital

    Essen, 45147
    Germany

    Active - Recruiting

  • Ammerland Klinik GmbH

    Westerstede, 26655
    Germany

    Active - Recruiting

  • Klinikum Worms gGmbH

    Worms, 67550
    Germany

    Active - Recruiting

  • Arcispedale Santa Maria Nuova

    Department of Neurology, ASMN IRCCS, Reggio Emilia 42123
    Italy

    Site Not Available

  • Arcispedale Santa Maria Nuova, Department of Neurology, ASMN IRCCS

    Reggio Emilia, 42123
    Italy

    Active - Recruiting

  • University Hospital Doctor Josep Trueta

    Girona, 17707
    Spain

    Active - Recruiting

  • Cantonal Hospital of Aarau

    Aarau, 5001
    Switzerland

    Active - Recruiting

  • Basel University Hospital

    Basel, 4031
    Switzerland

    Completed

  • Department of Neurology, Bern University Hospital, Bern

    Bern, 3010
    Switzerland

    Active - Recruiting

  • Geneva University Hospital

    Geneva, 1211
    Switzerland

    Active - Recruiting

  • Lausanne University Hospital

    Lausanne, 1011
    Switzerland

    Active - Recruiting

  • Zürich Triemli Hospital

    Zürich, 8063
    Switzerland

    Site Not Available

  • Zürich Triemli Hospital

    Zürich, 8063
    Switzerland

    Completed

  • Zürich University Hospital

    Zürich, 8091
    Switzerland

    Active - Recruiting

  • Tufts Medical Center

    Boston, Massachusetts 02111
    United States

    Active - Recruiting

  • Baystate Medical Center

    Springfield, Massachusetts 01199
    United States

    Completed

  • Mercy Hospital St. Louis

    St. Louis, Missouri 63141
    United States

    Site Not Available

  • East Medical Center

    Tyler, Texas 75710
    United States

    Active - Recruiting

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