Monitor Patients With Acute Heart Failure
Completed
- Conditions
- Heart Failure
- Registration Number
- NCT00919828
- Lead Sponsor
- Corventis, Inc.
- Brief Summary
This is a prospective, multi-center, non-randomized study to evaluate performance of an external monitor for heart failure patients
- Detailed Description
External monitoring of heart failure patients with the AVIVO System.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- Is female or male, 18 years of age or older
- Has an ejection fraction of 40% reported within 12 months of enrollment
- Having acute decompensated heart failure and receiving treatment for fluid overload
Exclusion Criteria
- Is participating in another clinical study that may confound the results of this study
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms does the AVIVO System monitor to assess heart failure progression in patients?
How does external monitoring with the AVIVO System compare to standard-of-care in managing acute heart failure?
Which biomarkers are most predictive of response to external monitoring in NCT00919828 heart failure study?
What adverse events are associated with long-term use of implantable cardiac monitoring devices in heart failure patients?
What are the current competitor devices to the AVIVO System for monitoring heart failure and how do they differ?