Post-resuscitation Care Registry for Survival From Out-of-hospital Cardiac Arrest

February 16, 2022 updated by: Jong Hwan Shin, Seoul National University Hospital
The aim of this study is to construct multi-center post-cardiac arrest care registry that can be used for data warehousing and clinical research.

Study Overview

Status

Completed

Detailed Description

This registry prospectively enrolls adults patients survived out-of-hospital cardiac arrest in 3 academic hospital emergency departments.

Registered data can be used for quality control and clinical research to reduce post-cardiac arrest syndrome-related mortality.

Study Type

Observational

Enrollment (Actual)

1057

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

      • Seongnam-si, Korea, Republic of, 13620
        • Seoul National University Bundang Hospital
      • Seoul, Korea, Republic of, 03080
        • Seoul National University Hospital
      • Seoul, Korea, Republic of, 07061
        • Seoul National University Boramae 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

20 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Patients with sustained ROSC from OHCA

Description

Inclusion Criteria:

  • Patients aged 20 years old or older who presents to the ED of the participating hospitals with any of the following criteria:

    1. Sustained ROSC from OHCA at pre-hospital level
    2. Sustained ROSC from OHCA at the ED of the participating hospitals after ACLS
    3. Patients sustained ROSC from OHCA and transferred from other hospital to the ED of the participating hospitals for post-cardiac arrest care

Exclusion Criteria:

  • Age less than 20 years old
  • Patients with advanced directives not to deliver aggressive organ supportive management

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Survival
Time Frame: 1-year
One year survival
1-year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
28-day mortality
Time Frame: 28-day
Mortality on the 28th day
28-day
28-day CPC
Time Frame: 28-day
Brain function at 28th day
28-day
6-month CPC
Time Frame: 6-month
Brain function at 6-month
6-month
1-year CPC
Time Frame: 1-year
Brain function at 1-year
1-year
Organ support treatment (mechanical ventilation)
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
Mechanical ventilation
Hospital discharge (non-survivors) or 1-year (survivors)
Organ support treatment (renal replacement therapy)
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
Renal replacement therapy
Hospital discharge (non-survivors) or 1-year (survivors)
ICU length of stay
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
ICU length of stay
Hospital discharge (non-survivors) or 1-year (survivors)
Hospital length of stay
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
Hospital length of stay
Hospital discharge (non-survivors) or 1-year (survivors)

Collaborators and Investigators

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

Investigators

  • Study Director: Jonghwan Shin, MD, PhD, Seoul National University Boramae Hospital

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)

December 3, 2013

Primary Completion (Actual)

December 31, 2019

Study Completion (Actual)

June 30, 2020

Study Registration Dates

First Submitted

June 8, 2018

First Submitted That Met QC Criteria

October 2, 2018

First Posted (Actual)

October 4, 2018

Study Record Updates

Last Update Posted (Actual)

February 18, 2022

Last Update Submitted That Met QC Criteria

February 16, 2022

Last Verified

February 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 16-2013-157

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.

Clinical Trials on Out-Of-Hospital Cardiac Arrest

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