RECRUITING

Inappropriate Sinus Tachycardia Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2022-03-01
Study Completion:2027-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05107635

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.

Ages Eligible for Study:Not specified
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Subject is scheduled to undergo or has undergone a procedure to treat IST or POTS using one or more AtriCure devices.
  2. 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. 1. Subject is enrolled in a concurrent study that may impact treatment outcome of IST or POTS.
  2. 2. Subject with exclusion criteria required by FDA or local governance

Contacts and Locations

Study Contact

Brianna Senior Registry Specialist
CONTACT
781-922-6107
bneil@atricure.com

Study Locations (Sites)

Stanford University
Palo Alto, California, 94305
United States
Sequoia Hospital
Redwood City, California, 94062
United States
University of Florida
Gainesville, Florida, 32608
United States
Sarasota Memorial Hospital
Sarasota, Florida, 34239
United States
Kansas City Cardiac Arrhythmia Research
Kansas City, Kansas, 64132
United States
MedStar Health Research Institute
Hyattsville, Maryland, 20782
United States
The Carl & Edyth Lindner Center for Research & Education at The Christ Hospital
Cincinnati, Ohio, 45219
United States
Texas Cardiac Arrhythmia Research Foundation
Austin, Texas, 78705
United States
Intermountain Medical Center
Murray, Utah, 84107
United States

Collaborators and Investigators

Sponsor: AtriCure, Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-03-01
Study Completion Date2027-01

Study Record Updates

Study Start Date2022-03-01
Study Completion Date2027-01

Terms related to this study

Keywords Provided by Researchers

  • Inappropriate Sinus Tachycardia
  • Postural Tachycardia Syndrome;
  • Sinus Node Sparing Hybrid Procedure

Additional Relevant MeSH Terms

  • Inappropriate Sinus Tachycardia
  • Postural Tachycardia Syndrome