Trials / Completed
CompletedNCT02501304
Feasibility Study of the ReVENT Sleep Apnea System
Feasibility Study of the ReVENT Sleep Apnea System for the Treatment of Obstructive Sleep Apnea (OSA)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Revent Medical International B.V. · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ReVENT Sleep Apnea System | The ReVENT Sleep Apnea System consists of minimally invasive biocompatible devices that are placed into the tongue base and palate of patients with obstructive sleep apnea |
Timeline
- Start date
- 2011-05-01
- Primary completion
- 2013-08-01
- Completion
- 2016-04-01
- First posted
- 2015-07-17
- Last updated
- 2016-11-04
Source: ClinicalTrials.gov record NCT02501304. Inclusion in this directory is not an endorsement.