Call to Door Timing in Out-of-hospital Cardiac Arrest

October 31, 2023 updated by: SungA Bae, Yonsei University

Clinical Impact in Patients With Delayed Hospitalization in Patients With Out-of-hospital Cardiac Arrest

The investigators aimed to investigate the effect of delayed hospitalization on the basis of the call time on the clinical outcomes of patients with OHCA patients using a nationwide OHCA registry.

Study Overview

Status

Completed

Conditions

Detailed Description

According to "2020 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care", immediate call for the local emergency response number takes a key role in the OHCA as the CPR in community does not provide quality of in-hospital CPR. The strong recommendation of speedy transportation, however, does not provide time limitation, and evident data supporting benefit within certain minutes to transfer is lack through our best of search. Therefore, The investigators aimed to investigate the effect of delayed hospitalization on the basis of the call time on the clinical outcomes of patients with OHCA patients using a nationwide OHCA registry.

Study Type

Observational

Enrollment (Actual)

182508

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Korea, Republic of
    • Giheung-gu
      • Yongin, Giheung-gu, Korea, Republic of, 16995
        • Yongin Severance Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Cardiac arrest with cardiopulmonary resuscitation

Description

Inclusion Criteria:

  • Out-of-hospital cardiac arrest event

Exclusion Criteria:

  • Arrest of non-cardiac origin
  • Age < 18 years
  • No any CPR
  • Missing data on call time

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Cardiac Arrest
Out-Of-Hospital Cardiac Arrest

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Death from any cause at hospital discharge
Time Frame: up to 30 days
Death from any cause at hospital discharge
up to 30 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Poor neurological outcomesat hospital discharge
Time Frame: up to 30 days
poor neurological outcomes, which was defined as a Glasgow-Pittsburge Cerebral Performance Category value at hospital discharge
up to 30 days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Yonsei University

Investigators

  • Principal Investigator: Yongcheol Kim, MD, PhD, Severance hospital, Yonsei university college of medicine

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 14, 2023

Primary Completion (Actual)

May 1, 2023

Study Completion (Actual)

October 24, 2023

Study Registration Dates

First Submitted

January 23, 2023

First Submitted That Met QC Criteria

February 1, 2023

First Posted (Actual)

February 13, 2023

Study Record Updates

Last Update Posted (Estimated)

November 3, 2023

Last Update Submitted That Met QC Criteria

October 31, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CtD timing

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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