Resuscitation Outcomes Consortium (ROC) Prehospital Resuscitation Using an Impedance Valve

NCT00394706 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 11738

Last updated 2018-08-09

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to look at two different treatments during a cardiac arrest that occurs outside of the hospital and whether either or both treatments will increase the number of people who live to hospital discharge. A cardiac arrest is when the heart stops pumping blood to the body.

Conditions

  • Heart Arrest

Interventions

DEVICE

Impedance Threshold Device (ITD)

Use of Impedance Threshold Device (ITD)

DEVICE

Sham ITD

Sham ITD

OTHER

Analyze early

Upon EMS arrival at the scene of a non-traumatic cardiac arrest, an assessment of the cardiac rhythm is done to determine whether a defibrillatory shock is required.

OTHER

Analyze later

Upon EMS arrival at the scene of a non-traumatic cardiac arrest, three minutes of CPR is given prior to the assessment of the cardiac rhythm to determine whether a defibrillatory shock is required.

Sponsors & Collaborators

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

    collaborator NIH
  • National Institute of Neurological Disorders and Stroke (NINDS)

    collaborator NIH
  • Canadian Institutes of Health Research (CIHR)

    collaborator OTHER_GOV
  • Defence Research and Development Canada

    collaborator INDUSTRY
  • Heart and Stroke Foundation of Canada

    collaborator OTHER
  • American Heart Association

    collaborator OTHER
  • University of Washington

    lead OTHER

Principal Investigators

  • Myron L Weisfeldt, MD · Johns Hopkins University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-06-30
Primary Completion
2009-11-30
Completion
2010-07-31

Countries

  • United States
  • Canada

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 NCT00394706 on ClinicalTrials.gov