MedTrace Logo

PREVENT - Prospective Rhythm Event Surveillance in the ER With NetGuard

NCT00750958 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 287

Last updated 2008-09-11

No results posted yet for this study

Summary

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.

Conditions

  • Cardiac Event

Interventions

PROCEDURE

NetGuard Automated Clinician Alert System

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

Sponsors & Collaborators

  • Datascope Patient Monitoring

    lead INDUSTRY

Principal Investigators

  • Charles Pollack, MD · Pennslvania Hospital

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2008-07-31
Completion
2008-07-31

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00750958 on ClinicalTrials.gov