NCT02473679

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,662

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2003

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2003

Completed
12.4 years until next milestone

First Submitted

Initial submission to the registry

May 13, 2015

Completed
1 month until next milestone

First Posted

Study publicly available on registry

June 16, 2015

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2016

Completed
Last Updated

November 2, 2016

Status Verified

November 1, 2016

Enrollment Period

13.5 years

First QC Date

May 13, 2015

Last Update Submit

November 1, 2016

Conditions

Keywords

First ResponderBLSAEDResuscitation

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability 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

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

Location

MeSH Terms

Conditions

Death, Sudden, CardiacHeart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular DiseasesDeath, SuddenDeathPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Donat R Spahn, Prof

    IFA, University Hospital Zurich

    PRINCIPAL INVESTIGATOR

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

Locations