Influence of the Education in Layperson in Out of Hospital Resuscitation

NCT ID: NCT02473679

Last Updated: 2016-11-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1662 participants

Study Classification

OBSERVATIONAL

Study Start Date

2003-01-31

Study Completion Date

2016-07-31

Brief Summary

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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).

Detailed Description

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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.

Conditions

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Cardiac Arrest, Sudden Heart Arrest

Keywords

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First Responder BLS AED Resuscitation

Study Design

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Observational Model Type

COHORT

Eligibility Criteria

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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

* 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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Zurich

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Donat R Spahn, Prof

Role: PRINCIPAL_INVESTIGATOR

IFA, University Hospital Zurich

Locations

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University Hospital Zurich

Zurich, Canton of Zurich, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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KEK2014 - 0665

Identifier Type: -

Identifier Source: org_study_id