Multicenter Study to Rule Out Myocardial Infarction by Cardiac Computed Tomography

NCT01084239 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2014-05-07

Study results available
· View outcomes & findings →

Summary

The growing availability of cardiac computed tomography (CT)\* in emergency departments (EDs) across the U.S. expands the opportunities for its clinical application, but also heightens the need to define its appropriate use in the evaluation of patients with acute chest pain. To address this need, we performed a randomized diagnostic trial (RDT) to determine whether integrating cardiac CT, along with the information it provides on coronary artery disease (CAD) and left ventricular (LV) function, can improve the efficiency of the management of these patients (i.e. shorten length of hospital stay, increase direct discharge rates from the ED, decreasing healthcare costs and improving cost effectiveness while being safe).

Conditions

Interventions

RADIATION

Cardiac Computed Tomography

A contrast enhanced cardiac CT was performed in addition to standard evaluation. Reconstructed data sets were evaluated for the presence of coronary artery calcium, coronary atherosclerotic plaque and stenosis, LV function and incidental findings.

Sponsors & Collaborators

  • National Heart, Lung, and Blood Institute (NHLBI)

    collaborator NIH
  • Kaiser Permanente

    collaborator OTHER
  • Beth Israel Deaconess Medical Center

    collaborator OTHER
  • Bay State Clinical Trials, Inc.

    collaborator OTHER
  • Washington University School of Medicine

    collaborator OTHER
  • Tufts Medical Center

    collaborator OTHER
  • The Cleveland Clinic

    collaborator OTHER
  • Northwestern University

    collaborator OTHER
  • University of Maryland

    collaborator OTHER
  • Massachusetts General Hospital

    lead OTHER

Principal Investigators

  • Udo Hoffmann, MD, MPH · Massachusetts General Hospital

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-04-30
Primary Completion
2012-01-31
Completion
2012-03-31

Countries

  • United States

Study Locations

More Related Trials

Entities

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 NCT01084239 on ClinicalTrials.gov