Monitoring Arrhythmia Patients in in Hospital Monitoring

This is a prospective, single center, non-randomized study to evaluate the arrhythmia monitoring performance of the AVIVO™ System in a hospital setting.

Completed

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Key information

Conditions

Arrhythmias Arrhythmias, Cardiac Cardiovascular Diseases Heart Diseases Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

The AVIVO™ System will continuously monitor the patient's cardiac activity which will be compared to the performance of standard telemetry 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
Undergoing in-hospital electrocardiographic monitoring for primarily cardiac reasons

Exclusion criteria

Is participating in another clinical study that may confound the results of this study

Sponsors and collaborators

Lead sponsor

Corventis, Inc.

Industry

Registry information

Official study title

Arrhythmia Detection With Adherent Patient Monitoring Study

Acronym: ADAM

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