Trials / Terminated
TerminatedNCT02152566
Nasal High Flow Therapy for the Treatment of Respiratory Insufficiencies During Sleep
Study of the Effects of Nasal High Flow Therapy as a Treatment Option for Patients With Respiratory Insufficiencies During Sleep.
- Status
- Terminated
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 6 (actual)
- Sponsor
- Fisher and Paykel Healthcare · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Respiratory insufficiencies during sleep can lead to reductions in the level of oxygen in the blood during the night, which has been shown to contribute to a range of morbidities. The purpose of this study is to assess the possibility that a nasal high flow therapy device may be able to treat respiratory insufficiencies, by stabilizing breathing and preventing reduction in blood oxygen. Heart failure patients will be screened at a heart failure clinic, and will be asked to undergo an overnight sleep study to determine is they exhibit respiratory insufficiencies during sleep. This sleep study may be completed in the sleep laboratory (attended polysomnography, PSG) or in-home (in-home polygraphy, PG). If they are diagnosed with respiratory insufficiencies, they will be asked to attend further overnight studies to see if treatment with nasal high flow therapy can be used to stabilize breathing.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Nasal High flow therapy device | Nasal high flow therapy via nasal cannula. |
Timeline
- Start date
- 2014-04-01
- Primary completion
- 2014-08-01
- Completion
- 2014-08-01
- First posted
- 2014-06-02
- Last updated
- 2016-02-08
- Results posted
- 2015-09-17
Locations
2 sites across 1 country: New Zealand
Source: ClinicalTrials.gov record NCT02152566. Inclusion in this directory is not an endorsement.