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NCT00750958 · ClinicalTrials.gov registry record · NA

PREVENT - Prospective Rhythm Event Surveillance in the ER With NetGuard

A NA study of Cardiac Event, sponsored by Datascope Patient Monitoring.

Completed
Registry status
NA
Development phase
287
Enrollment target
2
Study locations

NCT00750958 is a NA study of Cardiac Event that has completed, run by Datascope Patient Monitoring. The registered enrollment target is 287 participants, below the 993-participant average among 3 other Cardiac Event trials with a reported enrollment target (71% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT00750958, a NA study of Cardiac Event, has completed, sponsored by Datascope Patient Monitoring.

COMPLETED
Registry status
NA
Development phase
287 participants
Enrollment target
2
Study locations

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 Studied

Interventions

  • PROCEDURE NetGuard Automated Clinician Alert System

Study Locations (2)

Pennsylvania

  • Dr Charles Pollack - Philadelphia
  • University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 287 participants
Start Date 2008-06
Est. Completion 2008-07
Phase NA

Sponsor

Datascope Patient Monitoring

1 total trials

What the Registry Record Tells You About NCT00750958

The ClinicalTrials.gov registry entry for NCT00750958 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 287 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 993-participant average among 3 other Cardiac Event trials with a reported enrollment target (71% lower). The listed sponsor is Datascope Patient Monitoring, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Cardiac Event appearing as the primary indexed condition, and to 1 intervention - of which NetGuard Automated Clinician Alert System is the first listed.

NCT00750958 reports 2 study locations spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT00750958 about?

NCT00750958 is a clinical study titled "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.

What is the current status of trial NCT00750958?

This trial is currently completed. It is a NA study. The enrollment target is 287 participants. The study started on 2008-06. Estimated completion is 2008-07.

What conditions does trial NCT00750958 study?

This clinical trial studies the following conditions: Cardiac Event.

What interventions are being tested in trial NCT00750958?

The interventions under investigation include: NetGuard Automated Clinician Alert System (PROCEDURE).

Who is sponsoring clinical trial NCT00750958?

This trial is sponsored by Datascope Patient Monitoring, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00750958 being conducted?

This trial has 2 study locations across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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