Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07492420

MedCline Investigational Study for the Treatment of Mild OSA With Positional Therapy

Led by Amenity Health, Inc. · Updated on 2026-03-27

35

Participants Needed

1

Research Sites

30 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate the safety and effectiveness of the MedCline Sleep System in reducing symptoms related to mild OSA.

CONDITIONS

Official Title

MedCline Investigational Study for the Treatment of Mild OSA With Positional Therapy

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis with mild obstructive sleep apnea (AHI 5-14.9)
  • Sleep study (PSG or HST) performed within last 24 months
  • Age 18 years or older
  • Routinely sleep on a standard mattress and can accommodate a 30-inch wide pillow
  • Overall good health without significant medical conditions interfering with study or safe sleep
  • Ability to provide written informed consent
  • Stable on any medications for at least 3 months prior to consent
Not Eligible

You will not qualify if you...

  • Diagnosis of moderate or severe OSA (AHI >15) or central sleep apnea
  • Surgical procedures for sleep apnea within last six months
  • Significant cardiac or respiratory conditions affecting study or outcomes
  • Chronic pain or musculoskeletal disorders affecting comfortable side sleeping
  • Pregnant or planning pregnancy during study
  • Conditions causing frequent night-time awakenings
  • Unable or unwilling to use the MedCline Sleep System as required
  • Use of substances or medications that significantly alter sleep or breathing

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Clayton Sleep Institute

St Louis, Missouri, United States, 63123

Actively Recruiting

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Research Team

M

Matthew Uhles

CONTACT

N

Nicholas Bossaller

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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