Trials / Completed
CompletedNCT00493948
Evaluation of a Portable Device for Assessing Sleep Disordered Breathing in Congestive Heart Failure
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 35 (actual)
- Sponsor
- ResMed · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate an approved, portable device for assessing Sleep Disordered Breathing in Congestive Heart Failure.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | ApneaLink | A two channel sleep screening device for the assessment of Sleep Disordered Breathing. |
Timeline
- Start date
- 2007-07-01
- Primary completion
- 2009-04-01
- Completion
- 2009-04-01
- First posted
- 2007-06-29
- Last updated
- 2009-11-11
Locations
1 site across 1 country: Australia
Source: ClinicalTrials.gov record NCT00493948. Inclusion in this directory is not an endorsement.