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Not listed Not applicable Interventional

Study Using Negative Pressure to Reduce Apnea

ClinicalTrials.gov ID: NCT04861038

Public ClinicalTrials.gov record NCT04861038. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Study Using Negative Pressure to Reduce Apnea (SUPRA)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to determine the safety and effectiveness of the aerSleep® II device for treatment of moderate to severe Obstructive Sleep Apnea (OSA) over 24 weeks of home use in spontaneously breathing adult subjects who are intolerant of Continuous Positive Airway Pressure (CPAP) therapy.

Study identification

NCT ID
NCT04861038
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Sommetrics, Inc.
Industry
Enrollment
900 participants

Conditions and interventions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 29, 2021 (Actual)
Primary completion
Dec 2025 (Estimated)
Completion
Dec 2025 (Estimated)
Last update posted
Apr 16, 2024

2021 – 2025

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
University of Arizona Tucson Arizona 85719 —
Preferred Research Partners Little Rock Arkansas 72211 —
Infinitive Bioresearch Los Angeles California 90048 —
BetterNight San Diego California 92123 —
Delta Waves Colorado Springs Colorado 80918 —
Baptist Hospital Miami Florida 33176 —
Clayton Sleep Institute St Louis Missouri 63123 —
The MetroHealth System Cleveland Ohio 44109 —
Cleveland Clinic Foundation Cleveland Ohio 44195 —
The Ohio State University Columbus Ohio 43210 —
Thomas Jefferson University Philadelphia Pennsylvania 19107 —
UPMC Pittsburgh Pennsylvania 15213 —
Bogan Sleep Consultants Columbia South Carolina 29201 —
BioSerenity Columbia South Carolina 29212 —
Sleep Therapy & Research Center San Antonio Texas 78229 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04861038, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 16, 2024 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04861038 live on ClinicalTrials.gov.

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