Could a sleep apnea machine keep heart patients out of the hospital?
NCT ID NCT03647891
First seen Jul 20, 2026 · Last updated Jul 21, 2026 · Updated 1 time
Summary
This study investigates whether diagnosing and treating obstructive sleep apnea with CPAP therapy early, while patients are still in the hospital for heart problems, can reduce the chance of being readmitted within 30 days. The trial enrolls adults with heart failure, heart attack, or arrhythmia who also have sleep apnea. Participants receive CPAP, a device that keeps the airway open during sleep, and researchers track readmission rates and other health outcomes.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Continuous Positive Airway Pressure (CPAP) therapy
- What this could lead to
- If successful, early CPAP treatment could become a standard part of cardiac care to prevent hospital readmissions.
- What could go wrong
- This is a small, early-stage study without a control group, so results may not be conclusive. CPAP adherence can be low, which may limit its impact.
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.
- Expected to start
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Jul 2017
An estimate. Start dates often move.
- Finished
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Sep 2017
- 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 * Males or female, any race, and age 18 and older * OSA-predominant (AHI at or above 5) sleep disordered breathing * Primary diagnosis upon admission of congestive heart failure, acute coronary syndrome, or arrhythmias * Congestive heart failure (Acute or acute on chronic systolic heart failure, Acute or acute on chronic diastolic heart failure) * Acute coronary syndrome (ST segment elevation myocardial infarction, Non-ST segment myocardial infarction, Unstable angina) * Arrhythmias (Tachyarrhythmias, Atrial fibrillation, Atrial flutter, Bradyarrhythmias, Sinus bradycardia, 2nd degree atrioventricular block, Complete heart block) * Appropriate to perform portable sleep study while on room air (no oxygen) * Patients who are able and willing to give informed consent Exclusion Criteria: * Use of CPAP within 6 months of enrollment * Patients with CSA-predominant sleep disordered breathing * Patients who are "sleepy": ESS at or above 11 * Commercial driver's license or other occupational hazards (operating heavy machinery) * Non-English speaking (validated questionnaires are currently limited to English) * Patients with chronic respiratory failure requiring oxygen therapy or non-invasive ventilation. * Patients requiring tracheostomy * Pregnant patients
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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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