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Study identifier: NCT03821129 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

GORE® CARDIOFORM Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke in Patients With Patent Foramen Ovale (PFO): the REDUCE Post Approval Study

Condition: Stroke · PFO - Patent Foramen Ovale  ·  Sponsor: W.L.Gore & Associates

PhaseNA
Planned participants636
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

This study will assess the safety and effectiveness of GORE® CARDIOFORM Septal Occluder in a post approval setting and evaluate the quality of operator education and training and transferability of trial experience to a post-market setting.

This description comes directly from the study's public registry record.

Talk to the study team

Tammy DeLozier  ·  800-437-8181  ·  GSO1801@wlgore.com

Always discuss trial participation with your own doctor first.

Locations (45)

St. Mary's HospitalTucson, Arizona, United StatesWithdrawn
Scripps Health La JollaLa Jolla, California, United StatesRecruiting
Loma Linda University HealthLoma Linda, California, United StatesRecruiting
University of California - San FranciscoSan Francisco, California, United StatesRecruiting
Santa Barbara Cottage HospitalSanta Barbara, California, United StatesRecruiting
South Denver Cardiology AssociatesLittleton, Colorado, United StatesRecruiting
Medical Center of the RockiesLoveland, Colorado, United StatesRecruiting
Yale University School of MedicineNew Haven, Connecticut, United StatesRecruiting
Baptist Health JacksonvilleJacksonville, Florida, United StatesRecruiting
Naples Community HospitalNaples, Florida, United StatesRecruiting
University of SF (Tampa General Hospital)Tampa, Florida, United StatesRecruiting
Cleveland Clinic FloridaWeston, Florida, United StatesActive Not Recruiting

+ 33 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT03821129