Could a week of home monitoring beat a single night in the lab for sleep apnea?
NCT ID NCT03819361
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether monitoring oxygen levels at home for 14 nights gives a more accurate diagnosis of obstructive sleep apnea than the standard single-night test in a hospital. Researchers enrolled 130 adults with suspected sleep apnea. They compared results from home monitoring with the in-hospital sleep study to see if multiple nights reduce false positives and false negatives. The goal is to improve how sleep apnea is diagnosed and treated.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- pulse-oximetry (home sleep monitoring device)
- What this could lead to
- If successful, this could show that home monitoring over multiple nights gives a more accurate diagnosis of sleep apnea than a single-night hospital test.
- What could go wrong
- This is a small, completed study with 130 participants. It only tests diagnostic accuracy, not treatment outcomes, so the real-world impact on patient care is uncertain.
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
-
130 people
The number who actually took part.
- Started
-
Feb 2019
- Finished
-
Jul 2023
- Lead sponsor
-
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
Patients with suspected obstructive sleep apnea
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Informed consent * Suspected obstructive sleep apnea * ≥18 years old Exclusion Criteria: * Suspected or diagnosed sleeping-disordered breathing other than OSA * Moribund or severe disease prohibiting protocol adherence especially COPD GOLD III-IV and heart failure NYHA III-IV * Patients receiving oxygen therapy or home ventilation * Continuous positive airway pressure treatment for OSA at baseline * Physical or intellectual impairment precluding informed consent or protocol adherence * 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
-
University Hospital Zurich
Zurich, Canton of Zurich, 8091, Switzerland
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