Breath test may predict sleep apnea severity without needles
NCT ID NCT07606898
First seen Jun 25, 2026 · Last updated Aug 26, 2026 · Updated 3 times
Summary
This study is testing whether a simple breath test, called fractional exhaled nitric oxide (FeNO), can help measure the severity of obstructive sleep apnea (OSA). Researchers will compare FeNO levels in 200 adults with different levels of sleep apnea to see if the test can predict moderate to severe cases. If it works, this could give doctors a non-invasive way to assess airway inflammation and improve how sleep apnea is managed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple, non-invasive breath test to help diagnose and manage obstructive sleep apnea severity.
- What could go wrong
- This is an observational study, not a treatment trial. The breath test may not reliably predict sleep apnea severity, and results may not apply to smokers or people with other lung conditions.
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
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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May 2026
- Expected to finish
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Oct 2026
An estimate. End dates often move.
- 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
Study Type: prospective observational cross sectional study. Sample Size: This study will be carried out on 200 patients' suspected for obstructive sleep apnea, following approval of medical research ethical committee of Tanta University, Faculty of Medicine. Sample size was calculated using this formula 2SD \^2 × (1.96 + 0.84)\^2 /d\^2 SD of FeNO 50 at moderate OSA 17.25 d is the difference between both means 21, 13.57 So at power of study 80% CI 95% Least Sample size will be 85 in each group
- Ages
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18 to 70 years
- 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: * Ages Eligible for study: 18 years till 70 years old. * Newly suspected OSA patients with Epworth Sleepiness Scale (ESS) ≥ 10. Exclusion Criteria: * Current smokers. * Any chronic Respiratory disorders other than OSA (asthma, COPD, allergic rhinitis, and atopic diseases). * Younger age than 18 years. * Recent inhaled or systemic corticosteroids within the pasr 4 weeks. * Recent respiratory infection less than 4 weeks. * Uncontrolled diabetes \& any chronic debilitating diseases (liver, renal, collagen diseases) Informed Consent will be taken from the participants before clinical examination.
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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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Tanta University
Tanta, Egypt
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Other studies related to the condition(s) this trial covers.
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