Obstructive Sleep Apnea Clinical Trial
Official title:
The Evaluation of a Nasal Pillows Mask for the Treatment of Obstructive Sleep Apnea (OSA)
Verified date | April 2017 |
Source | Fisher and Paykel Healthcare |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This investigation is designed to evaluate the performance as well as the patients overall acceptance of the mask.
Status | Completed |
Enrollment | 22 |
Est. completion date | March 2017 |
Est. primary completion date | January 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Adult (18+ years of age) - Able to give consent - Apnea hypopnea Index (AHI)= 5 on diagnostic night - Prescribed PAP for OSA - Existing nasal pillows user Exclusion Criteria: - Inability to give consent - Patients who are in a coma or a decreased level of consciousness - Anatomical or physiological conditions making automatic positive airway pressure (APAP) therapy inappropriate (e.g. unconsolidated facial structure) - Commercial drivers who are investigated by New Zealand Transport Agency - Current diagnosis of carbon dioxide (CO2) retention - Pregnant or may think they are pregnant |
Country | Name | City | State |
---|---|---|---|
New Zealand | Fisher and Paykel Healthcare | Auckland | |
New Zealand | Hawkes Bay Fallen Soldiers' Memorial Hospital | Hastings |
Lead Sponsor | Collaborator |
---|---|
Fisher and Paykel Healthcare |
New Zealand,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Ease of use | Subjective questionnaire | 2 weeks in home | |
Primary | Acceptability | Subjective questionnaire | 2 weeks in home | |
Secondary | Objective leak data | Obtained from participants' device | 2 weeks in home |
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