Quality of Cardiopulmonary Resuscitation Without and With Defibrillator Feedback

Sponsor
University of Oslo (Other)
Overall Status
Completed
CT.gov ID
NCT00138996
Collaborator
Laerdal Medical (Industry), Ullevaal University Hospital (Other), Health Region East, Norway (Other), Norwegian Air Ambulance Foundation (Other), London Ambulance Service (Other), Stockholm Ambulance Service (Other), University of Chicago (Other)
300
3
51
100
2

Study Details

Study Description

Brief Summary

Quality of bystander cardiopulmonary resuscitation (CPR) affect patient survival. Quality of professional CPR on patients has not been studied in detail, but it is regularly reported that the quality when tested on manikins deteriorates dramatically within months after training. Automated direct feedback on CPR quality from manikins brings quality back within a couple of minutes. Similar feedback has been incorporated into a defibrillator which also monitors quality of CPR. We hypothesise that quality of professional clinical CPR improves with such feedback

Condition or Disease Intervention/Treatment Phase
  • Device: automated direct feedback on CPR from defibrillator
Phase 2

Detailed Description

Defibrillators which monitor quality of CPR via changes in thoracic impedance (for ventilation) and movement of the sternum employing an accelerometer (for chest compressions) will be employed in ambulances in Akershus county (Norway), Stockholm (Sweden) and London (UK). During phase 1 quality of CPR will be monitored without feedback from the defibrillator. During phase 2 the ambulance personnel will receive feedback via the defibrillator. During phase 3 the ambulance personnel will be retrained with particular attention to the quality problems that became apparent in phase 3.

Quality of CPR will be continuously recorded by the defibrillators and the data collected and sent via internet to Laerdal Medical. All other cardiac arrest data including survival will be recorded using standard datasets for cardiac arrest research as developed by a task force with members from the organisations in International Liaison Committee on resuscitation (Utstein guidelines). The data will be annotated and analyzed in detail by researchers at University of Oslo

Study Design

Study Type:
Interventional
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Can the Quality of Cardiopulmonary Resuscitation Improve With Direct Online Feedback From the Defibrillator to the Rescuers on Their Resuscitation Efforts
Study Start Date :
Mar 1, 2002
Actual Study Completion Date :
Jun 1, 2006

Outcome Measures

Primary Outcome Measures

  1. fraction of time without CPR []

  2. chest compression depth []

  3. chest compression frequency []

  4. chest compression/decompression duty cycle []

  5. ventilation frequency []

Secondary Outcome Measures

  1. rate of return of spontaneous circulation []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Cardiac arrest out-of-hospital
Exclusion Criteria:
  • < 18 years old

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ulleval University Hospital Oslo Norway N-0407
2 Stockholm Ambulance Service Stockholm Sweden
3 London Ambulance Service London United Kingdom

Sponsors and Collaborators

  • University of Oslo
  • Laerdal Medical
  • Ullevaal University Hospital
  • Health Region East, Norway
  • Norwegian Air Ambulance Foundation
  • London Ambulance Service
  • Stockholm Ambulance Service
  • University of Chicago

Investigators

  • Principal Investigator: Petter A Steen, University of Oslo, Ulleval University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00138996
Other Study ID Numbers:
  • 402-01139
  • 2002-OSL-MDD-0009 (DNVeritas)
First Posted:
Aug 30, 2005
Last Update Posted:
Aug 27, 2007
Last Verified:
Aug 1, 2007
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 27, 2007