A smart neck brace may replace CPAP for sleep apnea

NCT ID NCT07807124

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Sep 08, 2026 · Last updated Sep 09, 2026 · Updated 1 time

Summary

This trial tests a device called C-Lift, a neck brace with sensors that detect breathing pauses and low oxygen during sleep. When a problem is sensed, the brace inflates or deflates to open the airway. Researchers will enroll 10 adults with moderate to severe obstructive sleep apnea who have not been helped by CPAP. The study measures whether wearing the device overnight reduces breathing interruptions and improves how rested participants feel.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
C-Lift, a sensor-equipped neck brace that inflates and deflates to open the airway during sleep
What this could lead to
If it works, the C-Lift could offer a comfortable, non-invasive alternative to CPAP for people with sleep apnea who struggle with the mask.
What could go wrong
This is a very small early test with only 10 participants, so results may not apply broadly. The device may be uncomfortable or fail to keep the airway open consistently.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 10 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2027

An estimate. Start dates often move.

Expected to finish

Jan 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Diagnosis of moderate to severe OSA (≥16 AHI events per hour) * Previously failed/refused CPAP * Not currently/actively participating in treatment for OSA Exclusion Criteria: * Diagnosis of mild OSA (AHI\<15 events per hour) * Received treatment for OSA in the 2-weeks prior to the sleep-study EX: CPAP, other oral device * Received prior surgical treatment for OSA EX: hypoglossal nerve stimulation (NOT including Tonsillectomy) * Diagnosis of comorbid sleep disorder EX: Insomnia * History of other sleep-disordered breathing EX: central sleep apnea, hypoventilation syndrome * History of cervical spine injury/surgery * Currently receiving oxygen therapy * Baseline oxygen saturation \<90% * Currently pregnant * History of substance abuse * Neck circumference \>20 inches * Regular use of medications which can impact sleep-disordered breathing or related symptoms. EX: opioids, benzodiazepines, gabapentin, antipsychotics, amphetamines or other stimulants.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

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Contacts and locations

Locations

  • The Center for Sleep and Cardiovascular Outcomes Research (C-SCOR) Sleep Laboratory

    Pittsburgh, Pennsylvania, 15213, United States

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