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RECRUITING
NCT05537753
NA

Encore PFO Closure Device - The PerFOrm Trial

Sponsor: Encore Medical Inc.

View on ClinicalTrials.gov

Summary

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.

Official title: Encore PFO Closure Device U.S. IDE Randomized Trial - The PerFOrm Trial

Key Details

Gender

All

Age Range

18 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

500

Start Date

2023-07-12

Completion Date

2030-10

Last Updated

2024-09-19

Healthy Volunteers

No

Interventions

DEVICE

Encore PFO closure device

The Encore PFO closure device comprises an implant component and a single-use delivery system.

DEVICE

FDA-approved PFO closure device

Chosen by the investigator

Locations (8)

Arkansas Cardiology

Little Rock, Arkansas, United States

Southern CA Permanente Medical Group - Kaiser San Diego and Scripps Memorial Hospital

La Jolla, California, United States

University of South Florida

Tampa, Florida, United States

Mercy One Iowa Heart Center

West Des Moines, Iowa, United States

Kansas University Medical Center

Kansas City, Kansas, United States

Jackson Heart Clinic

Jackson, Mississippi, United States

CHI Health

Omaha, Nebraska, United States

Medical University of South Carolina Gazes Research Institute

Charleston, South Carolina, United States