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| Sponsored by: |
Corventis, Inc. |
| Information provided by: | Corventis, Inc. |
| ClinicalTrials.gov Identifier: | NCT00557804 |
Purpose
This is a multi-center, non-randomized study designed to develop an external monitor for CHF patients.
| Condition | Intervention |
|
Congestive Heart Failure |
Device: MUSE clinical system |
| MedlinePlus related topics: | Heart Failure |
| ChemIDplus related topics: | Alprostadil |
| Study Type: | Observational |
| Study Design: | Case-Only, Other |
| Official Title: | Multi-Sensor Monitoring in Congestive Heart Failure Study |
| Estimated Enrollment: | 362 |
| Study Start Date: | December 2007 |
| Estimated Study Completion Date: | February 2009 |
Heart failure patients will be externally monitored. The collected information will be used to assess patient status.
Eligibility
| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
primary care and heart failure clinics
Inclusion Criteria:
18 years of age or older
Contacts and Locations More Information
| Responsible Party: | Corventis ( Imad Libbus, PhD ) |
| Study ID Numbers: | COR-2007-001 |
| First Received: | November 9, 2007 |
| Last Updated: | April 2, 2008 |
| ClinicalTrials.gov Identifier: | NCT00557804 |
| Health Authority: | United States: Food and Drug Administration |
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