AtriCure Devices for Inappropriate Sinus Tachycardia
Inappropriate Sinus Tachycardia Registry
- Age
- 18 – 100
- Sex
- Any
- Study type
- Observational
- Participants needed
- 500 (estimated)
- Sponsor
- AtriCure, Inc. · Industry
This trial is looking for patients who are having a procedure to treat Inappropriate Sinus Tachycardia or Postural Tachycardia Syndrome using AtriCure devices. Participants will share their experience to help gather safety and performance data.
You may be able to join if
- I am having or will have a procedure to treat IST or POTS with AtriCure devices.
- I am willing to provide written consent to participate.
You may not be able to join if
- I am enrolled in another study that could affect my treatment outcome.
- I do not meet any FDA or local governance criteria.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your EligibilityThe 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.
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