Could a home device spot sleep apnea in people on narcotics?
NCT ID NCT03670914
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study tests whether a wearable home sleep apnea device called WatchPAT200 can accurately detect central sleep apnea in people who take narcotic medications. Participants wear the device during an overnight lab sleep study, and results are compared to the standard in-lab test. If the device works well, it could offer a more convenient way to diagnose sleep-related breathing problems in this group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- WatchPAT200 home sleep apnea test device
- What this could lead to
- If accurate, this could allow people on narcotics to be tested for sleep apnea at home instead of in a lab.
- What could go wrong
- This is a small, early study with only 24 participants, so results may not apply to everyone. The device may not detect all types of breathing events accurately.
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
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24 people
The number who actually took part.
- Started
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Aug 2019
- Finished
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Mar 2025
- 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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Accepted
You do not need to have the condition being studied to take part.
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 * Kaiser Permanente member * Patient is able to read, understand and sign the informed consent form. * Subject on current narcotic prescription with of at least 4 nights/week (subject will be asked on night of PSG if they took narcotic medication and specific medication taken) Exclusion Criteria * Finger deformity that precludes adequate sensor appliance * Use of one of the following medications: alpha blockers, short acting nitrates (less than 3 hours before the study) * Patients that are oxygen dependent * Patients with Chronic Obstructive Pulmonary Disease (COPD) with FEV1 \<70%, obesity hypoventilation syndrome, neuromuscular weakness
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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.
Contacts and locations
Locations
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Sleep Center; San Bernardino County Medical Center, Kaiser Permanente
Fontana, California, 92335, United States
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