Out-of-hospital Cardiopulmonary Resuscitation and AED Feedback

This study has been completed.

Sponsor:

Information provided by:

University Hospital Muenster

ClinicalTrials.gov Identifier:

NCT00449969

First received: March 20, 2007

Last updated: April 21, 2011

Last verified: April 2011

History of Changes

Tracking Information

First Received Date ^ICMJE

March 20, 2007

Last Updated Date

April 21, 2011

Start Date ^ICMJE

April 2007

Primary Completion Date

April 2009 (final data collection date for primary outcome measure)

Current Primary Outcome Measures ^ICMJE

ratio of patients with spontaneous circulation [ Time Frame: admission to the hospital ] [ Designated as safety issue: No ]

Original Primary Outcome Measures ^ICMJE

ratio of patients with spontaneous circulation until admission to the hospital

Change History

Complete list of historical versions of study NCT00449969 on ClinicalTrials.gov Archive Site

Current Secondary Outcome Measures ^ICMJE

length of hospital stay [ Time Frame: hospital discharge ] [ Designated as safety issue: No ]
neurological status [ Time Frame: hospital discharge ] [ Designated as safety issue: No ]
neurological status [ Time Frame: one year after resuscitation ] [ Designated as safety issue: No ]

Original Secondary Outcome Measures ^ICMJE

length of hospital stay
neurological status at hospital discharge
neurological status at one year after resuscitation

Current Other Outcome Measures ^ICMJE

Not Provided

Original Other Outcome Measures ^ICMJE

Not Provided

Descriptive Information

Brief Title ^ICMJE

Out-of-hospital Cardiopulmonary Resuscitation and AED Feedback

Official Title ^ICMJE

Quality of Out-of-hospital Cardiopulmonary Resuscitation (CPR) With Real Time Automated Feedback: a Prospective Randomized Study

Brief Summary

The purpose of this study is to determine whether an online automatic feedback improved CPR quality (No-flow time, compression depth, short-term survival and one year follow up) in this prospective randomised study of out-of-hospital cardiac arrest

Detailed Description

Not Provided

Study Type ^ICMJE

Interventional

Study Phase

Not Provided

Study Design ^ICMJE

Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment

Condition ^ICMJE

Cardiac Arrest
Resuscitation

Intervention ^ICMJE

Device: Zoll AED pro
Arm one (Extended feedback) offers full feedback guidance during CPR
Device: Zoll AED pro
In arm two (limited feedback) feedback is modified lacking several elements of feedback

Study Arm (s)

Experimental: 1. Extended feedback
Intervention: Device: Zoll AED pro
Active Comparator: 2. Limited feedback
Intervention: Device: Zoll AED pro

Publications *

* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information

Recruitment Status ^ICMJE

Completed

Enrollment ^ICMJE

312

Completion Date

December 2010

Primary Completion Date

April 2009 (final data collection date for primary outcome measure)

Eligibility Criteria ^ICMJE

Inclusion Criteria:

cardiac arrest

Exclusion Criteria:

age under 18 years

Gender

Both

Ages

18 Years and older

Accepts Healthy Volunteers

Contacts ^ICMJE

Contact information is only displayed when the study is recruiting subjects

Location Countries ^ICMJE

Germany

Administrative Information

NCT Number ^ICMJE

NCT00449969

Other Study ID Numbers ^ICMJE

02-AnIt-07

Has Data Monitoring Committee

Responsible Party

Thomas P. Weber, principle investigator, Department of Anesthesiology and Intensive Care

Study Sponsor ^ICMJE

University Hospital Muenster

Collaborators ^ICMJE

Not Provided

Investigators ^ICMJE

Study Chair:

Thomas P Weber, MD

Department of Anesthesiology and Intensive Care, University Hospital Muenster

Information Provided By

University Hospital Muenster

Verification Date

April 2011

^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

To Top