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Inappropriate Sinus Tachycardia Registry

Key facts

Where
Austin, Cincinnati, Gainesville, Hyattsville, Kansas City, Kissimmee, Loma Linda, Murray, Palo Alto, Redwood City, Sarasota, and Seattle, United StatesSee the 12 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 100 years old?

Source: NCT05107635, who can take part

Where in United States

  • Texas Cardiac Arrhythmia Research FoundationAustin, United StatesContact: Chantel ScallonTaking people
  • The Carl & Edyth Lindner Center for Research & Education at The Christ HospitalCincinnati, United StatesContact: Anne VoorhorstTaking people
  • University of FloridaGainesville, United StatesContact: Jessica CobbTaking people
  • MedStar Health Research InstituteHyattsville, United StatesContact: Katherine MahoneyTaking people
  • Kansas City Cardiac Arrhythmia ResearchKansas City, United StatesContact: Donita AtkinsTaking people
  • HCA Osceola Regional Medical CenterKissimmee, United StatesContact: Mary Janette SendinTaking people
  • Loma Linda University HealthLoma Linda, United StatesContact: Kisha-Nicole HefflinTaking people
  • Intermountain Medical CenterMurray, United StatesContact: Lindsey BevenTaking people
  • Stanford UniversityPalo Alto, United StatesContact: Tiffany KoyanoTaking people
  • Sequoia HospitalRedwood City, United StatesContact: Juanita FujiTaking people
  • Sarasota Memorial HospitalSarasota, United StatesContact: Alexandra GardnerTaking people
  • Swedish Health ServicesSeattle, United StatesContact: Faith OtewaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
AtriCure, Inc.
Trial code
NCT05107635
Record updated
7 October 2026
Original 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.Read full original descriptionShow less

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

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.

Inclusion: 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.

Exclusion: Subject is enrolled in a concurrent study that may impact treatment outcome of IST or POTS; Subject with exclusion criteria required by FDA or local governance.

ClinicalTrials.gov NCT05107635