Evaluation of the Quality of Cardio-Pulmonary Resuscitation (CPR) in Cardiac Arrest Patients

NCT00951704 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2018-12-13

No results posted yet for this study

Summary

The prognosis of cardiac arrest patients is generally poor. Recent studies have showed that the high quality of CPR increases the survival after cardiac arrest. Therefore the investigators planned this prospective observational study to determine the epidemiology of sudden cardiac arrest in the prehospital setting of Tampere area, the quality of the CPR, and also the associations between depth and frequency of chest compressions and invasive arterial pressure, EtCO2,cerebral oxygenation and iatrogenic injuries associated to chest compressions 1) in patients resuscitated out of hospital by emergency medical service's (EMS's) personals and 2) in-hospital by hospital resuscitation team members. In addition, the investigators will analyze the effects of the chosen method of resuscitation on critical vital signs (Etco2 and invasive pressures): closed-chest CPR is compared to open-chest CPR, or mechanical CPR with a device (AutoPulse-CPR, Cardio Pump) compared to manual CPR guided with quality CPR device. The results will give the investigators important insights into the haemodynamics of CPR which may guide future strategies for the management of cardiac arrest. The research group is also interested in CPR related injuries and mattress effect. Quality of life after CA is evaluated among survivals and the cause of death among non-survivors.

Conditions

  • Cardiac Arrest

Sponsors & Collaborators

  • Turku University Hospital

    collaborator OTHER_GOV
  • Uppsala University

    collaborator OTHER
  • Tampere University Hospital

    lead OTHER

Principal Investigators

  • Jyrki Tenhunen, MD, PhD · Critical Care Medicine Research Group

  • Sanna Hoppu, MD, PhD · Tampere University Hospital

  • Marko Sainio, MD · Turku University Hospital

  • Klaus Olkkola, MD, PhD · Department of Anesthesiology and Intensive Care, Helsinki University Hospital

  • Heidi Hellevuo, MD · Tampere University Hospital

  • Piritta Setälä, MD · Tampere University Hospital

  • Ilkka Virkkunen, MD, PhD · Tampere University Hospital

  • Heidi Kangasniemi, MD · Tampere University Hospital

  • Joonas Tamminen · Tampere University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-11-30
Primary Completion
2015-12-31
Completion
2018-12-31

Countries

  • Finland

Study Locations

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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 NCT00951704 on ClinicalTrials.gov