Encore PFO Closure Device - The PerFOrm Trial

Recruiting N/A Interventional Study
Patent Foramen Ovale Cryptogenic Stroke
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 60
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
500 (estimated)
Sponsor
Encore Medical Inc. · Industry
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About This Trial

The objective of this study is to establish reasonable assurance of safety, effectiveness, and noninferiority of the Encore PFO closure device when compared to any investigator chosen FDA-approved PFO closure device.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Diagnosis of PFO, defined as visualization of microbubbles per TEE in the left atrium within three cardiac cycles from the right atrial opacification demonstrating right-to-left shunting at rest and/or during Valsalva release 2. Cryptogenic stroke within the last 270 days; st…
Contacts

Joseph Marino

651-797-0913

jmarino@encore-medical.com

CONTACT

Hannah Bearinger

hannah.bearinger@brightresearch.com

CONTACT