SleepFlexTM Treatment of Obstructive Sleep Apnea
NCT04726514 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10
Last updated 2023-06-22
Summary
The purpose of this study is to evaluate the safety and effectiveness of the SleepFlex program for treatment of mild to moderate OSA
Conditions
Interventions
- DEVICE
-
SleepFlex
SleepFlex Program
Sponsors & Collaborators
-
Berendo Scientific, LLC
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 21 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-07-20
- Primary Completion
- 2022-04-01
- Completion
- 2022-05-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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