NCT06948266

Brief Summary

  • 1 PMC
  • 1 In the SYMPTOMS table, marked as cardiac arrest. In the ECG table, marked rhythms: VF/VT, Asystole, PEA. In the PATIENT MANAGEMENT table, marked: MANUAL CHEST COMPRESSIONS, MECHANICAL CHEST COMPRESSIONS, DEFIBRILLATION. In the DEATH-WITHDRAWAL table, information on the reason for discontinuing resuscitation efforts. Only adult patients will be included in the study. Available demographic data will include patient age, gender, and the territorial area of the medical event, indicated by the location of the call and the voivodeship.
  • Estimated Study Group Size
  • Estimated Study Duration

Trial Health

55
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

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, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

April 21, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

April 29, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2025

Completed
Last Updated

April 29, 2025

Status Verified

April 1, 2025

Enrollment Period

5 months

First QC Date

April 21, 2025

Last Update Submit

April 21, 2025

Conditions

Keywords

sudden cardiac deathpolandOHCA

Outcome Measures

Primary Outcomes (1)

  • OHCA

    Number of OHCA in Poland in 2023

    1 year

Study Arms (1)

OHCA

OHCA in Oland in 2023.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults (≥18 years) who experienced an OHCA in 2023, identified through MEPCs

You may qualify if:

  • Adults (≥18 years) who experienced an OHCA in 2023, identified through MEPCs containing at least one of the following indicators:
  • ICD-10 codes: I46, R98, R96 in the diagnosis section. Witness-reported initiation of CPR in the patient examination section. Indication of cardiac arrest in the symptoms table. Documented rhythms such as VF/VT, asystole, or PEA in the ECG table. Noted interventions like manual/mechanical chest compressions or defibrillation in the patient management table.
  • Reasons for cessation of resuscitation efforts in the death/discontinuation table.

You may not qualify if:

  • Individuals under 18 years of age.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Medical University of Gdańsk

Gdansk, 80-211, Poland

Location

MeSH Terms

Conditions

Death, Sudden, CardiacHeart DiseasesHeart Arrest

Condition Hierarchy (Ancestors)

Cardiovascular DiseasesDeath, SuddenDeathPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
phd

Study Record Dates

First Submitted

April 21, 2025

First Posted

April 29, 2025

Study Start

January 1, 2025

Primary Completion

June 1, 2025

Study Completion

July 1, 2025

Last Updated

April 29, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will share

Yes, individual participant data (IPD) that underlie the results reported in this study will be made available upon reasonable request. Interested researchers may contact the corresponding author via email to obtain access, contingent upon appropriate data use agreements and ethical approvals.

Shared Documents
STUDY PROTOCOL, SAP
Time Frame
From 12.2025
Access Criteria
Who will have access: Access will be granted to researchers affiliated with academic institutions, hospitals, or other non-commercial research organizations, who demonstrate a legitimate scientific interest in the study topic. All requestors must have appropriate ethics approval for secondary data use if required by their institution or jurisdiction.

Locations