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remedē System Therapy Study — reST  

Central Sleep Apnea Clinical Trial

Official title:
Prospective Non-randomized Post Market Study Collecting Clinical Data on Safety and Effectiveness of the remedē® System

Clinical Trial Summary

The purpose of this non-randomized post market study is to collect clinical data on the safety and effectiveness of the remedē System in a real-world setting.

Clinical Trial Description

This is a multi-center, prospective, open label, non-randomized study to collect safety and effectiveness data in subjects with central sleep apnea implanted with the remedē System. At least 500 subjects will be successfully implanted at approximately 50 sites in the United States and Europe. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03884660
Study type Observational
Source Respicardia, Inc.
Contact Kimberly Guilbault
Phone 260-348-9035
Email kim.guilbault@zoll.com
Status Recruiting
Phase
Start date June 18, 2019
Completion date June 30, 2032
View Details
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