Monitor Patients With Acute Heart Failure

Adherent Monitoring of Congestive Heart Failure During Therapy for Excess Fluid Study

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00919828

Acronym

ACUTE

Enrollment

Registered

2009-06-12

Start date

2009-03-31

Completion date

2009-12-31

Last updated

2010-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

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.

Interventions

DEVICEAvivo System

Non invasive external monitoring device

Study design

Observational model

CASE_ONLY

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026