Influence of the Education in Layperson in Out of Hospital Resuscitation
1 other identifier
observational
1,662
1 country
1
Brief 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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2003
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2003
CompletedFirst Submitted
Initial submission to the registry
May 13, 2015
CompletedFirst Posted
Study publicly available on registry
June 16, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2016
CompletedNovember 2, 2016
November 1, 2016
13.5 years
May 13, 2015
November 1, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Time line for restoration the circulation
Timeline for restoration the circulation after layperson started the reanimation
participants will be followed from origin of the event up to 12 month or death
Secondary Outcomes (4)
Time interval to first shock ,
participants will be followed from origin of the event up to 12 month or death
Neurologic outcome
participants will be followed from origin of the event for duration of hospital stay, follow up after 12 month or death
Time interval removal from ICU as well as discharged from hospital
participants will be followed from origin of the event up to 12 month or death
Definitive survival rate
participants will be followed from origin of the event up to 12 month or death
Eligibility Criteria
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
You may qualify if:
- All Out of hospital patients suffering cardiac arrest in Zurich City, resuscitated by lay persons, city police and or trained emergency medical services
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Zurich
Zurich, Canton of Zurich, 8091, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Donat R Spahn, Prof
IFA, University Hospital Zurich
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
May 13, 2015
First Posted
June 16, 2015
Study Start
January 1, 2003
Primary Completion
July 1, 2016
Study Completion
July 1, 2016
Last Updated
November 2, 2016
Record last verified: 2016-11