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ACTIVE NOT RECRUITING
NCT03732794
NA

AtriCure CryoICE Lesions for Persistent and Long-standing Persistent Atrial Fibrillation Treatment

Sponsor: AtriCure, Inc.

View on ClinicalTrials.gov

Summary

The primary objective of this study is to evaluate the safety and effectiveness of the AtriCure CryoICE system in performing the Cox-Maze III lesion set, in conjunction with Left Atrial Appendage (LAA) exclusion using the AtriClip device.

Official title: AtriCure CryoICE Lesions for Persistent and Long-standing Persistent Atrial Fibrillation Treatment During Concomitant On-Pump Endo/Epicardial Cardiac Surgery

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

150

Start Date

2019-01-30

Completion Date

2026-06

Last Updated

2024-10-15

Healthy Volunteers

No

Interventions

DEVICE

AtriCure CryoICE & AtriClip LAA Exclusion

AtriCure CryoICE system in performing the Cox-Maze III lesion set, in conjunction with LAA exclusion using the AtriClip device.

Locations (15)

UCLA Medical Center

Los Angeles, California, United States

Washington Adventist Hospital

Washington D.C., District of Columbia, United States

Northwestern Medicine

Chicago, Illinois, United States

Franciscan Health

Indianapolis, Indiana, United States

Deaconess Gateway Hospital

Newburgh, Indiana, United States

University Of Maryland

Baltimore, Maryland, United States

University of Michigan

Ann Arbor, Michigan, United States

Mayo Clinic

Rochester, Minnesota, United States

St. Luke's Hospital

Kansas City, Missouri, United States

Mount Sinai Icahn School of Medicine

New York, New York, United States

NYP-Weill Cornell

New York, New York, United States

Northwell Health Systems

New York, New York, United States

St. Joseph Hospital Health Center

Syracuse, New York, United States

St Thomas West Hospital

Nashville, Tennessee, United States

West Virginia University

Morgantown, West Virginia, United States