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CompletedNCT02473679Updated Nov 2, 2016

Influence of the Education in Layperson in Out of Hospital Resuscitation

An observational study in Cardiac Arrest, Sudden and Heart Arrest, sponsored by University of Zurich. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-11-02.

Sponsored by University of Zurich · Observational

Study type
Observational
Model
Cohort
Enrollment
1,662
Ages
18 Years and older
Sex
All
01

Study summary

Cardiac arrest occurs frequently and the outcome after out-of-hospital resuscitation is often fatal. Disturbing is that more than half of the surviving patients suffer from permanent impairment of cognitive functions, such attention, memory and executive functioning. With all the efforts to achieve a high quality initial resuscitation management the time delay between cardiac arrest and the beginning the initial resuscitation maneuver is the main reason for the still poor outcome. To shorten this fatal time delay, current efforts of national and supranational health authorities aime at the non-medically trained lay person, who should carry out basic life support directly on the scene supported by the use of public available semi-automatic defibrillators (AED).

Read the detailed description

It is a combined retrospective and prospective observational single center study. Data of all Out of Hospital patients suffered a cardiac arrest in Zurich city will be collected according to the Utstein criteria. The aim of this study is to investigate the impact of trained police forces in the resuscitation outcome.

02

Conditions studied

  • Cardiac Arrest, Sudden
  • Heart Arrest

Keywords

  • First Responder
  • BLS
  • AED
  • Resuscitation
03

In context

Heart Arrest

966 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's enrollment of 1,662 is above the median of 200 across 383 observational studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

University of Zurich is the lead sponsor of 1,030 studies on the registry; 130 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Out of hospital patients suffered or suffering cardiac arrest, who were or will be resuscitated by laypersons, city police and/or trained emergency medical services teams who were called to the emergency

Inclusion criteria

  • All Out of hospital patients suffering cardiac arrest in Zurich City, resuscitated by lay persons, city police and or trained emergency medical services

Exclusion criteria

Exclusion Criteria:

  • individuals with cardiac arrest occurring in the presence of EMS
  • individuals in whom there were apparent toxic, traumatic or suicidal etiologies for unconsciousness
  • drowned individuals and individuals with terminal illness
  • documented negation of data collection
05

Study design

Observational model
Cohort
Enrollment
1,662 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Time line for restoration the circulation

    Timeline for restoration the circulation after layperson started the reanimation

    Time frame: participants will be followed from origin of the event up to 12 month or death

Secondary outcomes

  1. Time interval to first shock ,

    Time interval from the emergency call to first shock for ventricular fibrillation

    Time frame: participants will be followed from origin of the event up to 12 month or death

  2. Neurologic outcome

    Data will be collected according to Utstein criteria

    Time frame: participants will be followed from origin of the event for duration of hospital stay, follow up after 12 month or death

  3. Time interval removal from ICU as well as discharged from hospital

    Time interval up to the removal from ICU as well as duration of hospital stay

    Time frame: participants will be followed from origin of the event up to 12 month or death

  4. Definitive survival rate

    Survival rate of participants resuscitated by layperson after cardiac arrest

    Time frame: participants will be followed from origin of the event up to 12 month or death

07

Study locations

1 site
  • University Hospital Zurich
    Zurich, 8091, Switzerland
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 2, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02473679
Lead sponsor
University of Zurich
Responsible party
Sponsor
First posted
Jun 16, 2015
Start date
Jan 2003
Primary completion
Jul 2016
Completion
Jul 2016
Last update
Nov 2, 2016

Study contacts

Donat R Spahn, Prof
principal investigator · IFA, University Hospital Zurich

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Nov 2016. You cannot join it, but the record below documents what was studied.

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