A Multicenter Patient Registry for Outcomes of Inappropriate Sinus Tachycardia and Postural Orthostatic Tachycardia Syndrome Treatment
Status: Recruiting
Location: See all (10) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
The primary objective of this registry is to capture real-world safety and performance data on AtriCure devices used to ablate cardiac tissue when treating Inappropriate Sinus Tachycardia (IST) or Postural Tachycardia Syndrome (POTS). This is a retrospective and prospective, multicenter, US/OUS, observational data registry.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Subject is scheduled to undergo or has undergone a procedure to treat IST or POTS using one or more AtriCure devices.
• Subject is willing to provide written informed consent (defined as legally effective, documented confirmation of a subject's voluntary agreement to participate in this Registry) or authorization per institution and geographical requirements
Locations
United States
California
Stanford University
RECRUITING
Palo Alto
Sequoia Hospital
RECRUITING
Redwood City
Florida
University of Florida
RECRUITING
Gainesville
Sarasota Memorial Hospital
RECRUITING
Sarasota
Kansas
Kansas City Cardiac Arrhythmia Research
RECRUITING
Kansas City
Maryland
MedStar Health Research Institute
RECRUITING
Hyattsville
Ohio
The Carl & Edyth Lindner Center for Research & Education at The Christ Hospital
RECRUITING
Cincinnati
Texas
Texas Cardiac Arrhythmia Research Foundation
RECRUITING
Austin
Utah
Intermountain Medical Center
RECRUITING
Murray
Other Locations
Belgium
Universitair Ziekenhuis Brussels
RECRUITING
Brussels
Contact Information
Primary
Brianna Senior Registry Specialist
IST-Registry@atricure.com
7819226107
Time Frame
Start Date: 2022-03-01
Estimated Completion Date: 2027-01
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Leads: AtriCure, Inc.