- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03695718
Post-resuscitation Care Registry for Survival From Out-of-hospital Cardiac Arrest
Study Overview
Status
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Seongnam-si, Korea, Republic of, 13620
- Seoul National University Bundang Hospital
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Seoul, Korea, Republic of, 03080
- Seoul National University Hospital
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Seoul, Korea, Republic of, 07061
- Seoul National University Boramae Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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:
- Sustained ROSC from OHCA at pre-hospital level
- Sustained ROSC from OHCA at the ED of the participating hospitals after ACLS
- 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
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
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28-day
|
6-month CPC
Time Frame: 6-month
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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)
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Mechanical ventilation
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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
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Hospital discharge (non-survivors) or 1-year (survivors)
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ICU length of stay
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
|
ICU length of stay
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Hospital discharge (non-survivors) or 1-year (survivors)
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Hospital length of stay
Time Frame: Hospital discharge (non-survivors) or 1-year (survivors)
|
Hospital length of stay
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Hospital discharge (non-survivors) or 1-year (survivors)
|
Collaborators and Investigators
Investigators
- Study Director: Jonghwan Shin, MD, PhD, Seoul National University Boramae Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 16-2013-157
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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