A Study of the Sleepnet Elara APAP Device

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSleepnet Corporation

About this trial

The goal of this study is to evaluate the effectiveness of the Elara APAP device.

Eligibility criteria

Qualifiers

Body weight ≥ 30kg

Willing and able to consent, adhere to study requirements and receive mask treatment

≥ 18 years of age

Diagnosed with OSA (Total AHI >15 events/hr) by a practicing physician within the last 6 months. A re-diagnosis may be necessary to establish current baseline AHI in case there has been significant weight change or other co-morbidities since the previous diagnosis (per PI discretion)

Disqualifiers

Body weight < 30kg

Female currently bearing a child or intending to become pregnant prior to the sleep study.

Have implanted pacemaker, ICD or any other medical device that would interfere with the PSG results or safety of the subject undergoing the study

Has pneumothorax, pneumomediastinum

Trial design

Treatments tested in this trial

  • Sleepnet Elara Treatment

Treatment groups

55 Participants
are divided into 1 treatment group

Sponsors and collaborators