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Effectiveness of the EMPOWER™ Modular Pacing System and EMBLEM™ Subcutaneous ICD to Communicate Antitachycardia Pacing — MODULAR ATP  

Tachycardia, Ventricular Clinical Trial

Official title:
Effectiveness of the EMPOWER™ Modular Pacing System and EMBLEM™ Subcutaneous ICD to Communicate Antitachycardia Pacing

Clinical Trial Summary

The MODULAR ATP Clinical Study is designed to demonstrate safety, performance, and effectiveness of the Modular Cardiac Rhythm Management (mCRM) Therapy System.

Clinical Trial Description

The MODULAR ATP Clinical Study will enroll subjects with a standard Implantable Cardioverter Defibrillator (ICD) indication applying international practice guidelines, as well as those who already have an implanted S-ICD System and satisfy the inclusion criteria for this study, while not meeting any exclusion criteria. Subjects will be followed for at least 6 months following mCRM Therapy System implantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04798768
Study type Interventional
Source Boston Scientific Corporation
Contact
Status Active, not recruiting
Phase N/A
Start date July 20, 2021
Completion date December 31, 2030
View Details
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