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COMPLETED NA

PREVENT - Prospective Rhythm Event Surveillance in the ER With NetGuard

NCT00750958 · View on ClinicalTrials.gov ↗

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

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00750958

The ClinicalTrials.gov registry entry for NCT00750958 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 287 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Datascope Patient Monitoring, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00750958 reports 2 study locations spanning 1 distinct geographic area — top geographies include Pennsylvania. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00750958?

The interventions under investigation include: NetGuard Automated Clinician Alert System (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00750958?

This trial is sponsored by Datascope Patient Monitoring, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

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