Recruiting

Observational Study

Sponsor:

Insel Gruppe AG, University Hospital Bern

Code:

NCT00859885

Conditions

Stroke

Transient Ischemic Attack

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Antithrombotic treatment

percutaneous device closure of PFO

Study Details

Brief 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.

Conditions

Stroke

Transient Ischemic Attack

Study ID

NCT00859885

Start date

Sep 8, 2008

Status verified date

Dec, 2017

Completion date

Dec, 2021

Anticipated

Primary completion date

Dec, 2021

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Enrollment

1500 participants

Anticipated

Interventions and Outcome Measures

Arms

1

Patients who receive antithrombotic treatment only

2

Patients who undergo percutaneous device closure

Interventions

Antithrombotic treatment

antiplatelets, anticoagulants

percutaneous device closure of PFO

umbrella device for PFO closure

Primary outcome measure

  • proportion of patients free of any stroke (including fatal stroke) or TIA [ Time Frame: 3 years ]

Central Contacts and Locations

Central contacts

Locations

Tufts Medical Center

Recruiting

Boston, Massachusetts, United States, 02111

East Medical Center

Recruiting

Tyler, Texas, United States, 75710

More Information

Sponsor

Insel Gruppe AG, University Hospital Bern

Last update posted

Dec 12, 2017

Last verified

Dec, 2017

Keywords

  • patent foramen ovale
  • ischemic stroke
  • transient ischemic attack
  • secondary prevention
  • medical treatment
  • percutaneous device closure

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Insel Gruppe AG, University Hospital Bern on 2017-12-12.