Monitor Patients With Acute Heart Failure

This is a prospective, multi-center, non-randomized study to evaluate performance of an external monitor for heart failure patients

Completed

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Key information

Conditions

Heart Failure Cardiovascular Diseases Heart Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

External monitoring of heart failure patients with the AVIVO System.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Avivo System

Device

Non invasive external monitoring device

Other names: external monitoring systems

Sponsors and collaborators

Lead sponsor

Corventis, Inc.

Industry

Registry information

Official study title

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

Acronym: ACUTE

Important dates

Study start: 2009
Primary completion: 2009
Study completion: 2009
First posted: Jun 12, 2009
Registry last updated: Feb 4, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed