Clinical trial
Evaluation of a Portable Device for Assessing Sleep Disordered Breathing in…
NCT00493948 · ResMed, Industry · Completed
Key facts
| NCT number | NCT00493948 |
|---|---|
| Title | Evaluation of a Portable Device for Assessing Sleep Disordered Breathing in Congestive Heart Failure |
| Official title | Evaluation of a Portable Device for Assessing Sleep Disordered Breathing in Congestive Heart Failure |
| Lead sponsor | ResMed, Industry |
| Status | Completed |
| Study type | Observational |
| Conditions | Heart Failure, Congestive, Sleep Apnea Syndromes |
| Intervention type | Device |
| Interventions | ApneaLink |
| Enrollment | 35 |
| Start date | Jul 1, 2007 |
| Primary completion | Apr 1, 2009 |
| Completion | Apr 1, 2009 |
| First posted | Jun 29, 2007 |
| Last update posted | Nov 11, 2009 |
| Countries | Australia |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: