NPA-OSA Device Tolerability, Usability and Acclimation Clinical Study in Adult Obstructive Sleep Apnea (OSA) Patients

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Michigan

About this trial

This pilot study is being done to determine if the nasopharyngeal airway obstructive sleep apnea (NPA-OSA) device can be used in the treatment of OSA in adults. The researchers think that the NPA-OSA device will reduce the number of apneas.

Eligibility criteria

Qualifiers

Capacity and willingness to sign consent

Patient willingness to commit to and complete study over a 30-day time period

Confirmed diagnosis of moderate to severe OSA (AHI >= 15)

OSA caused by upper airway obstruction

Disqualifiers

Within 3 months of initiating CPAP use, and actively using CPAP

Supraglottic airway collapse

Distal airway stenosis

Tracheobronchomalacia

Trial design

Treatments tested in this trial

  • nasopharyngeal airway obstructive sleep apnea (NPA-OSA) device

Treatment groups

20 Participants
are divided into 1 treatment group

Sponsors and collaborators

University of Michigan

Lead sponsor

Wallace H Coulter Center for Translational Research

Collaborator