A single center, prospective study to assess the efficacy of high flow nasal cannula (HFNC)
in improving obstructive sleep apnea (OSA) parameters in patients with reduced tolerance to
continuous positive airway pressure (CPAP) treatment.
Device: High flow nasal cannula
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Full eligibility criteria for NCT03017859
Ages eligible for Study
18 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
Age 18-80 years
Confirmed diagnosis of obstructive sleep apnea, diagnosed at RMC sleep lab in the past 2 years
Apnea Hypopnea Index (AHI)≥15
Patient has difficulties to adjust or comply with CPAP treatment
Signed Informed Consent Form
Patients who need bilevel positive airway pressure (BIPAP)
Known carbon dioxide (CO2) retainers
Weight change>10% compared to time of OSA diagnosis
Clinically unstable patients
Pregnant women or special populations (e.g. children or patients unable to give informed consent)
All locations for NCT03017859
View full eligibility
Tris trial is registered with FDA with number: NCT03017859. The sponsor of the trial is Rabin Medical Center and it is looking for 30 volunteers for the current phase.
Official trial title: High Flow Nasal Cannula as a Treatment for Obstructive Sleep Apnea
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