- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06218329
TIMECARD(TaIwan Network of Post-arrest ManagEment for CARDiac Arrest)IIRegistry (TIMECARDII)
January 22, 2024 updated by: National Taiwan University Clinical Trial Center
TIMECARD (TaIwan Network of Post-arrest ManagEment for CARDiac Arrest) II Registry
This study aims to collect the post-cardiac arrest patients with ICU admission.
Study Overview
Status
Recruiting
Detailed Description
The purpose of this study is to establish protocolized and standard post-arrest care as well as constitute a multicenter registry of post-arrest survivors, and thus to develop the Taiwan predictive model of cardiac arrest survivors.
The registry system may help evaluate the severity of disease illness and improve the post-arrest care.
Study Type
Observational
Enrollment (Estimated)
1000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Chien-Hua Huang
- Phone Number: 262831 2312-3456
- Email: chhuang5940@ntu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan, 100
- Recruiting
- Department of Emergency Medicine, National Taiwan University Hospital
-
Contact:
- Chien-Hua Huang
- Phone Number: 262831 2312-3456
- Email: chhuang5940@ntu.edu.tw
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
This study will enroll patients with who arrived at the emergency department with non-traumatic and admitted to the ICU.
Description
Inclusion Criteria:
- non-traumatic cardiac arrest patients
- Admitted to the ICU
Exclusion Criteria:
- Below 18 year old
- Pregnant
- Terminal illness or not receiving medical treatment
- When emergency ICU crowded can not provide Critical Care
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 |
Time Frame |
|---|---|
|
Number of cases
Time Frame: 2024/12/31
|
2024/12/31
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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)
January 1, 2022
Primary Completion (Estimated)
December 31, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
October 17, 2023
First Submitted That Met QC Criteria
January 22, 2024
First Posted (Actual)
January 23, 2024
Study Record Updates
Last Update Posted (Actual)
January 23, 2024
Last Update Submitted That Met QC Criteria
January 22, 2024
Last Verified
October 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202201091RINB
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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