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

March 20, 2007
April 21, 2011
April 2007
April 2009   (final data collection date for primary outcome measure)
ratio of patients with spontaneous circulation [ Time Frame: admission to the hospital ] [ Designated as safety issue: No ]
ratio of patients with spontaneous circulation until admission to the hospital
Complete list of historical versions of study NCT00449969 on ClinicalTrials.gov Archive Site
  • 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 ]
  • length of hospital stay
  • neurological status at hospital discharge
  • neurological status at one year after resuscitation
Not Provided
Not Provided
 
Out-of-hospital Cardiopulmonary Resuscitation and AED Feedback
Quality of Out-of-hospital Cardiopulmonary Resuscitation (CPR) With Real Time Automated Feedback: a Prospective Randomized Study

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

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Cardiac Arrest
  • Resuscitation
  • 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
  • Experimental: 1. Extended feedback
    Intervention: Device: Zoll AED pro
  • Active Comparator: 2. Limited feedback
    Intervention: Device: Zoll AED pro

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
312
December 2010
April 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • cardiac arrest

Exclusion Criteria:

  • age under 18 years
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00449969
02-AnIt-07
No
Thomas P. Weber, principle investigator, Department of Anesthesiology and Intensive Care
University Hospital Muenster
Not Provided
Study Chair: Thomas P Weber, MD Department of Anesthesiology and Intensive Care, University Hospital Muenster
University Hospital Muenster
April 2011

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