drugset / Trial / NCT00738894

GORE® Septal Occluder Device for Patent Foramen Ovale (PFO) Closure in Stroke Patients

NCT00738894

Completed 664 enrolled W.L.Gore & Associates
RandomizedParallel-groupSingle-blindTreatment

Summary

The primary objective is to determine if patent foramen ovale (PFO) closure with the GORE® HELEX® Septal Occluder or GORE® CARDIOFORM Septal Occluder plus antiplatelet medical management is safe and effective and reduces the risk of recurrent stroke or imaging-confirmed transient ischemic attack (TIA) when compared to antiplatelet medical management alone in patients with a PFO and history of cryptogenic stroke or imaging-confirmed TIA. A co-primary objective is to demonstrate that medical management plus closure with the study device reduces the risk of new brain infarct compared to medical management alone.

Timeline

Start
2008-12-10
Primary completion
2017-04-24
Completion
2020-05-11

Drugs

EvaluationDrugModalityDoseRoute
Background Aggrenox Unknown
Background Aspirin Small molecule
Background Clopidogrel Small molecule
Background Dipyridamole Other / unclassified