NCT05107635

Inappropriate Sinus Tachycardia Registry

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

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 500 (estimated)
• Sponsor: AtriCure, Inc. · Industry
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

Summary

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

Interventions

Type	Name	Description
DEVICE	AtriCure Commercially Available Devices	Epicardial and endocardial hybrid ablation procedure used to treat the IST or POTS using AtriCure commercially available devices.

Timeline

• Start date: 2022-03-01
• Primary completion: 2027-01-01
• Completion: 2027-01-01
• First posted: 2021-11-04
• Last updated: 2025-10-20

Locations

10 sites across 2 countries: United States, Belgium

Regulatory

• FDA-regulated device study