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Telemetry for Chest Pain of Low Risk for Acute Coronary Syndrome Pts

NCT02330328 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2020-01-13

No results posted yet for this study

Summary

This is a randomized controlled, multi-center, non-blinded non-inferiority study examining the utility of telemetry monitoring in patients admitted who are low risk for acute coronary syndrome. Each of the six sites will prospectively enroll 250 patients in each arm of the study randomized to either a med-surg bed (no telemetry) or a telemetry bed during their admission. Research study coordinators will enroll patients and then follow them throughout their hospital course and record primary and secondary end point events.

Conditions

  • Chest Pain
  • Telemetry
  • Acute Coronary Syndrome
  • Health Care Resource Utilization

Interventions

OTHER

No Telemetry Monitoring

DEVICE

Telemetry Monitoring

Sponsors & Collaborators

  • Johns Hopkins University

    collaborator OTHER

  • University of Maryland, College Park

    collaborator OTHER

  • Virginia Commonwealth University

    collaborator OTHER

  • Medstar Health Research Institute

    collaborator OTHER

  • Virginia Tech Carilion School of Medicine and Research Institute

    collaborator OTHER

  • Carilion Clinic

    lead OTHER

Principal Investigators

  • John Perkins, MD · Carlion Clinic

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
49 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2017-06-30
Completion
2017-07-31

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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 NCT02330328 on ClinicalTrials.gov