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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03695718
Other study ID # 16-2013-157
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 3, 2013
Est. completion date June 30, 2020

Study information

Verified date February 2022
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 1057
Est. completion date June 30, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility 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 Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam-si
Korea, Republic of Seoul National University Boramae Hospital Seoul
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (3)

Lead Sponsor Collaborator
Seoul National University Hospital Seoul National University Bundang Hospital, SMG-SNU Boramae Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survival One year survival 1-year
Secondary 28-day mortality Mortality on the 28th day 28-day
Secondary 28-day CPC Brain function at 28th day 28-day
Secondary 6-month CPC Brain function at 6-month 6-month
Secondary 1-year CPC Brain function at 1-year 1-year
Secondary Organ support treatment (mechanical ventilation) Mechanical ventilation Hospital discharge (non-survivors) or 1-year (survivors)
Secondary Organ support treatment (renal replacement therapy) Renal replacement therapy Hospital discharge (non-survivors) or 1-year (survivors)
Secondary ICU length of stay ICU length of stay Hospital discharge (non-survivors) or 1-year (survivors)
Secondary Hospital length of stay Hospital length of stay Hospital discharge (non-survivors) or 1-year (survivors)
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