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RECRUITING
NCT06689839
NA

Trial of the F2 Filter and Delivery System for Embolic Protection During TAVR

Sponsor: EnCompass Technologies, Inc.

View on ClinicalTrials.gov

Summary

The objective of this study is to compare the safety and effectiveness of the F2 Cerebral Protection System (CPS) to a standard of care control group in patients undergoing Transcatheter Aortic Valve Replacement (TF TAVR)

Official title: A Prospective, Randomized, Multicenter, Single-blind Trial to Assess the Safety and Effectiveness of the Encompass F2 Cerebral Protection System Vs. Standard of Care (Unprotected or Sentinel® Cerebral Protection System) During Transfemoral Transcatheter Aortic Valve Replacement

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

500

Start Date

2025-09-09

Completion Date

2027-01

Last Updated

2025-11-20

Healthy Volunteers

No

Interventions

DEVICE

F2 Filter and Delivery System

Use of the F2 Filter and Delivery System in conjunction with a Transcatheter Aortic Valve Replacement (TAVR) procedure

PROCEDURE

Transcatheter Aortic Valve Replacement (TAVR)

Transcatheter Aortic Valve Replacement (TAVR) with commercially available Transcatheter Aortic Valve Replacement (TAVR) device

Locations (10)

NCH Baker Hospital-Naples Heart Institute

Naples, Florida, United States

St. Vincent Hospital

Indianappolis, Indiana, United States

Henry Ford Hospital

Detroit, Michigan, United States

St. Lukes Hospital Of Kansas City

Kansas City, Missouri, United States

Cumc/Nyph

New York, New York, United States

Cleveland Clinic Foundation

Cleveland, Ohio, United States

Ohio Health Research Institute (aka Riverside Methodist Hospital)

Columbus, Ohio, United States

University of Virginia Medical Center

Charlottesville, Virginia, United States

St Andrews War Memorial Hospital

Spring Hill, Queensland, Australia

Monash Health Public

Clayton, Victoria, Australia