Severe OSA Study (SOS)
NCT05445869 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35
Last updated 2024-04-18
Summary
This study is a prospective, multi-center, single-arm, open-label study evaluating the safety and effectiveness of therapy with the ProSomnus EVO Sleep and Snore Device in individuals with severe obstructive sleep apnea.
Conditions
Interventions
- DEVICE
-
ProSomnus® EVO Sleep and Snore Device
The ProSomnus® EVO Sleep and Snore Device is an intraoral device for snoring and obstructive sleep apnea. It works by repositioning the mandible during sleep, thereby improving the flow of air through the patient's pharyngeal space. The ProSomnus® EVO Sleep consists of maxillary and mandibular device arches that are CAD/CAM designed with twin-mated posts and digitally milled to be patient-specific according to physician prescription. Prescribed advancements can be achieved by simply removing the current upper or lower device arch and inserting the next upper or lower device arch in the mandibular advancement series. The device does not have any adjustment mechanisms to modify or maintain the mandibular position such as pistons, screws, straps, or repositioning elastics. The device is supplied nonsterile.
Sponsors & Collaborators
-
ProSomnus Sleep Technologies
lead INDUSTRY
Principal Investigators
-
Erin Mosca, PhD · ProSomnus Sleep Technologies
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-09-12
- Primary Completion
- 2024-02-15
- Completion
- 2024-02-15
- FDA Device
- Yes
Countries
- United States
Study Locations
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