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Feasibility Study of the ReVENT Sleep Apnea System — REV-001  

Obstructive Sleep Apnea (OSA) Clinical Trial

Official title:
Feasibility Study of the ReVENT Sleep Apnea System for the Treatment of Obstructive Sleep Apnea (OSA)

Clinical Trial Summary

This is a prospective, multi-center, single arm, feasibility study to evaluate the safety and effectiveness of the ReVENT Sleep Apnea System for the treatment of Obstructive Sleep Apnea.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02501304
Study type Interventional
Source Revent Medical International B.V.
Contact
Status Completed
Phase N/A
Start date May 2011
Completion date April 2016
View Details
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