Sleep apnea patients stop CPAP for 2 weeks – Here's what scientists learned
NCT ID NCT05920083
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study involved 65 adults with obstructive sleep apnea who had been using CPAP therapy for at least 6 months. Participants stopped using CPAP for 2 weeks so researchers could measure changes in blood vessel function and nerve control of the heart. The goal was to see if a specific sleep measurement could predict how the body responds to stopping treatment.
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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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65 people
The number who actually took part.
- Started
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Jan 2024
- Finished
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Sep 2024
- 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: * Age ≥18 years old * Diagnosed with OSA (AHI ≥15 events/h), confirmed during screening period * Adequately treated with CPAP therapy for ≥6 months * Able to give informed consent as documented by signature Exclusion Criteria: * Professional drivers will be excluded from the study because temporary withdrawal of CPAP may induce drowsiness. * We will also exclude patients with conditions that may affect endothelial and autonomic function: * Known Diabetes * Known heart failure * Known chronic kidney disease * Pregnant or lactating women * Morbid obesity (≥40 kg/m2) * Known Excessive alcohol consumption * Known Dementia (especially dementia with Lewy bodies). (61) * Patients using alpha and beta blockers * Known atrial fibrillation * Inability to follow the procedures of the study due to language problems or psychological disorders.
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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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Lausanne University Hospital
Lausanne, Canton of Vaud, 1012, Switzerland
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Real-world evaluation of the clinical performance and safety of apneal dx for the screening and aid in the diagnosis of obstructive sleep apnea-hypopnea syndrome in adults: a post-market clinical follow-up study
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