Monitoring Arrhythmia Patients (IMPACT)

Prospective, multicenter, non-randomized study to determine the performance of NUVANT Mobile Cardiac Telemetry system in arrhythmia detection.

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

Primary location

Dr. Bedi

Steubenville, Ohio, 43952, United States

About this study

Arrhythmia patients will be externally monitored. The collected information will be used to evaluate the NUVANT MCT system.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

18 years of age or older
Patients undergoing remote ambulatory electrocardiographic monitoring

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

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