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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 Sep 4, 2026, 1:16 AM 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 28, 2021
Primary completion
Nov 30, 2025
Completion
Nov 30, 2025
Last update posted
Apr 15, 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 15, 2024 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04861038 live on ClinicalTrials.gov.

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