MIHS Emergency Department CPR Quality Improvement Project

This study is currently recruiting participants. (see Contacts and Locations)
Verified August 2014 by Maricopa Integrated Health System
Information provided by (Responsible Party):
Maricopa Integrated Health System
ClinicalTrials.gov Identifier:
First received: November 19, 2010
Last updated: August 13, 2014
Last verified: August 2014

The investigators will quantify the quality of chest compressions provided in the Emergency Department and determine whether the quality of chest compressions is related to patient outcome. The quality of chest compressions and patient outcomes will be assessed both before and after the introduction of audiovisual feedback in real time.

Cardiac Arrest

Study Type: Observational
Study Design: Time Perspective: Prospective
Official Title: MIHS Emergency Department CPR Quality Improvement Project

Resource links provided by NLM:

Further study details as provided by Maricopa Integrated Health System:

Primary Outcome Measures:
  • CPR quality [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Measurement of chest compression depth and rate

Secondary Outcome Measures:
  • Health care outcomes [ Time Frame: 12 months ] [ Designated as safety issue: Yes ]
    Mortality and the following adverse events: infection, bleeding, DVT, hyperkalemia

Estimated Enrollment: 150
Study Start Date: November 2010
Estimated Study Completion Date: June 2018
Estimated Primary Completion Date: January 2018 (Final data collection date for primary outcome measure)
Detailed Description:

The Emergency Department will be using E-series unit manufactured by ZOLL Medical Group (Chelmsford, MA). These units are equipped with an accelerometer-based system that allows for measurement of chest compression depth and rate. These units are also equipped with RealCPRHelp, and FDA-approved technology that provides real-time audiovisual feedback to providers on the quality of chest compressions.

In the first phase of the project, the ED providers will utilize the E-series units to treat all patients requiring chest compressions.


Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients admitted to the ED who require chest compressions


Inclusion Criteria:

  • 18 years old or older

Exclusion Criteria:

  • less than 18 years old
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01245699

Contact: Bentley J Bobrow, MD 602-344-5417 bentley_bobrow@dmgaz.org
Contact: David A Drachman, PhD 602-344-5161 david.drachman@mihs.org

United States, Arizona
Maricopa Integrated Health System Recruiting
Phoenix, Arizona, United States, 85008
Sponsors and Collaborators
Maricopa Integrated Health System
Principal Investigator: Bentley J Bobrow, MD Maricopa Integrated Health System
  More Information

Responsible Party: Maricopa Integrated Health System
ClinicalTrials.gov Identifier: NCT01245699     History of Changes
Other Study ID Numbers: 2010-037
Study First Received: November 19, 2010
Last Updated: August 13, 2014
Health Authority: United States: Institutional Review Board

Keywords provided by Maricopa Integrated Health System:
Cardiac arrest, CPR, quality improvement

Additional relevant MeSH terms:
Heart Arrest
Cardiovascular Diseases
Heart Diseases

ClinicalTrials.gov processed this record on October 23, 2014