PREVENT - Prospective Rhythm Event Surveillance in the ER With NetGuard

Datascope

Status: Completed

Conditions: Cardiac Event

Treatments: Procedure: NetGuard Automated Clinician Alert System

Study type: Interventional

Funder types: Industry

Identifiers

NCT00750958

807119

Details and patient eligibility

About

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.

Enrollment: 287 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

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

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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287 participants in 1 patient group

1

No Intervention group

Description:

ED patients that are not monitored with conventional therapy.

Treatment:

Procedure: NetGuard Automated Clinician Alert System