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Active, not recruiting Observational

Fractional Exhaled Nitric Oxide as Possible Non - Invasive Biomarker to Assess Obstructive Sleep Apnea Severity

NCT07606898 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2026-05-25
Last updated
2026-08-25

Condition(s) studied

Obstructive Sleep Apnea (OSA)

Study summary

Aim of work

1. Primary aim: Asses correlation between FeNO level, OSA severity
2. Secondary aim: Clarifying FeNO's role as a biomarker to assess airway inflammation, Cut off value prediction to moderate and severe OSA and its potential significance to improve clinical management strategies for OSA patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
Accepted
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.

Primary outcome measure(s)

  • Asses correlation between FeNO level, OSA severity• through measuring FeNo level in 3 groups which will be divided according to AHI in PSG study -Control group AHI less than 5 \ hour, Mild OSA group AHI than 5-15 \ hour, Moderate to severe OSA group — baseline
    address the correlation between PSG parameters performed by Somno medics screen including (apnea hypopnea index (event\\ hour) oxygen nadir(%), oxygen desaturation index, % of time desaturation below 90% (T90), snoring index) and FeNo level ppb which measured by (Bedfont NIN006187 Nobreath) to Clarify FeNO's role as a biomarker to assess airway inflammation, and OSA severity, address FeNoCut off value as prediction tool to moderate and severe OSA and its potential significance to improve clinical management strategies for OSA patients. FeNo measurement precaution will be addressed as the participants will be asked to abstain from eating, drinking, and exercise, and avoid exposure to tobacco fumes 60 minutes before testing, so all cases FeNO assay will be hold at 9 am, Ask patients to refrain from Intake of nitrate-containing food like green-leaved vegetables on the day of assessment and then will be interprated according to ATS guidelines

Trial sites (1)

FacilityCityRegionStatus
Tanta University Tanta Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07606898 on ClinicalTrials.gov ↗ ← All trials in Egypt