New implant aims to stop sleep apnea in its tracks
NCT ID NCT06556693
First seen Oct 31, 2025 · Last updated Jun 23, 2026 · Updated 37 times
Summary
This study is testing a new device called the remedē Dual Channel System for people with severe sleep apnea. The device is implanted in the body and uses mild electrical stimulation to keep the airway open during sleep. The study will enroll 40 participants to see if the device is safe and can improve breathing. It is an early-stage feasibility study, so the main goals are to check safety and see if the device works as intended.
Disclaimer
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This is a summary of
the original study
.
Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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The Insomnia and Sleep Institute of Arizona LLC
RECRUITINGScottsdale, Arizona, 85255, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Contact
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The Ohio State University
RECRUITINGColumbus, Ohio, 43210, United States
Contact Email: •••••@•••••
Contact
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The University of Michigan Health-West
RECRUITINGWyoming, Michigan, 49519, United States
Contact Email: •••••@•••••
Contact
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
implantable dual channel stimulation device
What this could lead to
If successful, this device could offer a new treatment option for people with severe sleep apnea, potentially improving their breathing and sleep quality.
What could go wrong
This is an early feasibility study with only 40 participants, so results may not apply to everyone. The device requires surgery to implant, which carries risks like infection or nerve injury.
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.