This registry is collecting information on how well AtriCure commercially available devices work and how safe they are when used to treat Inappropriate Sinus Tachycardia (IST) or Postural Tachycardia Syndrome (POTS). IST and POTS are conditions that can cause a fast heartbeat. The study is looking at people who are already scheduled to have, or have had, a procedure using AtriCure devices to treat their IST or POTS. The main goal is to see how these devices perform over 12 months. This is an observational study, meaning researchers will collect data from real-world use. The current status of the study is unclear, but it aims to include about 500 participants.

Study design

This is an observational study, meaning researchers will collect information from people already undergoing treatment, rather than assigning treatments. It aims to include about 500 participants.

What's involved

You would need to be willing to provide written informed consent to participate in this registry.

Compensation

Not stated in the trial record.

Follow-up

The primary endpoint is measured at 12 months, suggesting participants will be followed for at least this duration after their procedure.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.