European Registry of Cardiac Arrest - Study Three
- Conditions
- out-of-hospital cardiac arrest of all causes
- Registration Number
- DRKS00028591
- Lead Sponsor
- niversitätsklinikum Schleswig-Holstein, Institut für Rettungs- und Notfallemdizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 47973
All patients who have an out of hospital cardiac arrest * and are attended by the EMS at any stage during the event. This study will include all events that occur between 00:00 on 1st September 2022 and 23:59 on 30th November 2022. Patients will be included irrespective of their age, gender or personal factors. These inclusion criteria include all patients who receive resuscitation (chest compression, and/or defibrillation of any type)
• By the EMS
• Before the arrival of the EMS with continued resuscitation by the EMS
• Before the arrival of the EMS, that is immediately stopped (for any reason) when the EMS arrives
• Patients who achieve ROSC before the arrival of the EMS
It also includes patients found or declared dead (for any reason).
Some countries or registries may not be able to provide all necessary data to answer every research question. These registries will not be included in the analysis of the related research questions.
no out-of-hopsital caridac arrest detected
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To enhance the key quality requirements of comprehensiveness and reliability, the aims of the EuReCa THREE project will be as follows:<br>• Expand the EuReCa network<br>• Improve the understanding of how response time and transport time influence return of spontaneous circulation (ROSC) and survival<br>• Overview of the longitudinal changes since EuReCA ONE <br>• Continue collecting data on established data-points/items to strengthen the robustness of European data collection
- Secondary Outcome Measures
Name Time Method To achieve these aims, the following objectives will be fulfilled:<br>• Encourage participating countries to aim for national data collection and encourage additional countries to participate<br>• To provide robust estimates of incidence, management and outcome, the data collection period will be three months (1st September to 30th November 2022)<br>• Identify consistency and variation in the measurement of time points and time intervals in connection with response times<br>• Describe the time intervals of response time and transport time