Actively Recruiting

Phase Not Applicable
Age: 8Years +
All Genders
NCT04446585

Cardiac Arrest in Residential Areas With Mobile First-responder Activation

Led by Emergency Medical Services, Capital Region, Denmark · Updated on 2023-09-15

260

Participants Needed

1

Research Sites

265 weeks

Total Duration

On this page

Sponsors

E

Emergency Medical Services, Capital Region, Denmark

Lead Sponsor

T

TrygFonden, Denmark

Collaborating Sponsor

AI-Summary

What this Trial Is About

The study aims to increase proportions of bystander defibrillation during out-of-hospital cardiac arrest (hereof referred to as cardiac arrest) in residential areas with a high density of cardiac arrests. The intervention consists of Automated External Defibrillators (AEDs) and residents' involvement in resuscitation through training and enrollment as citizen responders.

CONDITIONS

Official Title

Cardiac Arrest in Residential Areas With Mobile First-responder Activation

Who Can Participate

Age: 8Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All witnessed cardiac arrests registered in the Danish Cardiac Arrest Registry occurring within the study sites
  • Witnessed cardiac arrest
  • Non-traumatic cause of cardiac arrest, excluding intoxication, drowning, or suicide
Not Eligible

You will not qualify if you...

  • Cardiac arrest occurring in a nursing home
  • Cardiac arrest not treated by emergency medical services due to ethical reasons or obvious signs of death
  • Cardiac arrest suspected but not confirmed
  • Cardiac arrests witnessed by emergency medical personnel

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Emergency Medical Services Copenhagen

Ballerup Municipality, The Capital Region, Denmark, 2750

Actively Recruiting

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Research Team

A

Anne J Jørgensen, MD

CONTACT

F

Fredrik Folke, MD, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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