Not yet recruiting NCT07622082

Out-of-hospital Cardiac Arrest Epidemiology and Outcomes in Western Lithuania 2022-2028

— Observational Out-of-hospital Cardiac Arrest (OHCA)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied: The protocol lists: Protocol based.
Who it may be relevant to: Registry conditions: Out-of-hospital Cardiac Arrest (OHCA). Basic parameters: from 18 years · All.
What needs checking: Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place: Center list to be confirmed — check the primary protocol.
Next step: Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Prehospital Processess Optimization and Emergency Medical Services' Dispatcher's Actions Modeling Impact on Quality of Cardiopulmonary Resuscitation After Sudden Cardiac Arrest

Overview

Out-of-hospital cardiac arrest rate is common problem, because of high mortality rate. It is not clear incidence rate, epidemiology and outcomes in Lithuania

Detailed description

This data reported according to UTSTEIN guidelines could be compared with other countries from the region although not much data is available, but it will be a baseline for future references about processes in patient management, demographics, incidence rate and OHCA outcomes.

Interventions

Behavioral Protocol based
change of EMS dispatcher protocol

Primary outcome measures

The detection of death will be shorter [Time frame: 1st Jan 2030]

Secondary outcome measures (1)

The survival rate will increase [Time frame: 1st Jan 2030]

Eligibility criteria

Inclusion criteria

people experiencing out-of-hospital cardiac arrest

Exclusion criteria

all others

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model: Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07622082 · LITCPR

Primary sources (government registries)

ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗