Inappropriate Sinus Tachycardia Registry

Description

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.

Conditions

Inappropriate Sinus Tachycardia, Postural Tachycardia Syndrome

Study Overview

Study Details

Study overview

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.

A Multicenter Patient Registry for Outcomes of Inappropriate Sinus Tachycardia and Postural Orthostatic Tachycardia Syndrome Treatment

Inappropriate Sinus Tachycardia Registry

Condition
Inappropriate Sinus Tachycardia
Intervention / Treatment

-

Contacts and Locations

Palo Alto

Stanford University, Palo Alto, California, United States, 94305

Redwood City

Sequoia Hospital, Redwood City, California, United States, 94062

Gainesville

University of Florida, Gainesville, Florida, United States, 32608

Sarasota

Sarasota Memorial Hospital, Sarasota, Florida, United States, 34239

Kansas City

Kansas City Cardiac Arrhythmia Research, Kansas City, Kansas, United States, 64132

Hyattsville

MedStar Health Research Institute, Hyattsville, Maryland, United States, 20782

Cincinnati

The Carl & Edyth Lindner Center for Research & Education at The Christ Hospital, Cincinnati, Ohio, United States, 45219

Austin

Texas Cardiac Arrhythmia Research Foundation, Austin, Texas, United States, 78705

Murray

Intermountain Medical Center, Murray, Utah, United States, 84107

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Subject is scheduled to undergo or has undergone a procedure to treat IST or POTS using one or more AtriCure devices.
  • 2. 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
  • 1. Subject is enrolled in a concurrent study that may impact treatment outcome of IST or POTS.
  • 2. Subject with exclusion criteria required by FDA or local governance

Ages Eligible for Study

to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

AtriCure, Inc.,

Study Record Dates

2027-01