A smart neck brace may replace CPAP for sleep apnea
NCT ID NCT07807124
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
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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
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jan 2029
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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The Center for Sleep and Cardiovascular Outcomes Research (C-SCOR) Sleep Laboratory
Pittsburgh, Pennsylvania, 15213, United States
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