PREVENT - Prospective Rhythm Event Surveillance in the ER With NetGuard

The purpose of this study is to determine the incidence of clinically significant rhythm and rate changes in ED patients who are not placed on conventional telemetry, and to test the user-friendliness of a automated clinician alter device in hectic and noisy setting of a busy emergency room.

Completed

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Key information

Conditions

Cardiac Event Cardiovascular Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Dr Charles Pollack, Philadelphia, Pennsylvania, United States

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

> 18 yes
Agree to participate in study
Telemetry not indicated
Telemetry not available
Willingness to complete a questionnaire-

Exclusion criteria

Refusal to participate
Know sensitivity to adhesive
Language/communication barriers
Perceived high risk for lack of study compliance

Treatment and study plan

NetGuard Automated Clinician Alert System

Procedure

Monitoring System for in-hospital patients who are typically unmonitored. Identifies and alarms for cardiac rhythm changes.

Other names: NetGurard Automated Clinican Alert Systemm

Primary outcomes

Incidence of clinically significant rhythm and rate changes in ED patients.

Time frame: Patient ED stay

Secondary outcomes

Measure of user-friendliness of the device.

Time frame: Patient ED stay

Sponsors and collaborators

Lead sponsor

Datascope Patient Monitoring

Industry

Registry information

Acronym: PREVENT

Important dates

Study start: 2008
Primary completion: 2008
Study completion: 2008
First posted: Sep 11, 2008
Registry last updated: Sep 11, 2008

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