Clinical Trial

IOS Parameters and PAP Titration Pressure in Obstructive Sleep Apnea

Study acronym: IOS-PAP
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
This prospective observational study aims to investigate whether impulse oscillometry (IOS)-a non-invasive lung function test-can help predict the specific pressure settings needed for positive airway pressure (PAP) therapy in patients with obstructive sleep apnea (OSA). Currently, finding the optimal therapeutic pressure for OSA patients typically requires a titration process during sleep. This study explores if IOS parameters, which measure airway resistance and elasticity through small pressure oscillations during normal breathing, correlate with the final titration pressures (CPAP, EPAP, IPAP, and ΔP) determined by polysomnography. Adult patients diagnosed with moderate-to-severe OSA (Apnea-Hypopnea Index ≥ 15) will undergo standard diagnostic sleep testing followed by IOS testing using the Vyaire Vyntus BodyBox® system. The researchers will evaluate whether these respiratory measurements can accurately predict required airway pressures and if they can help clinicians distinguish between patients who need Continuous Positive Airway Pressure (CPAP) versus Bilevel Positive Airway Pressure (BPAP) therapy.
Trial Details
NCT Number NCT07554430
Lead Sponsor Mustafa Kemal University
Conditions Obstructive Sleep Apnea (OSA)
Enrollment 92 participants
Start Date 2026-05-01
Primary Completion 2026-11-30 (estimated)
Study Completion 2027-01-02 (estimated)
Updated on ClinicalTrials.gov 2026-04-28