Does heart surgery trigger sleep apnea? a study tracks its course
NCT ID NCT02632162
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This study follows 450 patients who recently had cardiac surgery to see how often sleep disordered breathing occurs and whether it changes over time. Researchers screen participants with the ApnoeLink Air device at the start of cardiac rehabilitation, again after 3 weeks, and at 3 months after surgery. The goal is to understand the natural course of sleep apnea in this group, which could inform future care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Screening with the ApnoeLink Air device to detect sleep disordered breathing
- What this could lead to
- If this trial succeeds, it could clarify how often sleep apnea occurs after cardiac surgery and whether it resolves on its own, guiding future screening and treatment decisions.
- What could go wrong
- This is an observational study, so it won't test any treatment. The results may not apply to all heart surgery patients, and the screening device may not be perfectly accurate.
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.
- Participants
-
About 450 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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May 2016
- Finished
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Dec 2020
- 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.
Who is studied
cardiac surgery \< 2 weeks
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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: * cardiac surgery or orthopedic surgery \<2 weeks Exclusion Criteria: * known SDB
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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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Zürcher RehaZentrum Wald
Wald, 8636, Switzerland
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