- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04875260
Taiwan Center of Outcome and Resource Evaluation
Taiwan Center of Outcome and Resource Evaluation Adult Intensive Care Units Database
The main purpose of this proposal is to build a multicenter de-identification adult intensive care units database in Taiwan. In future, the Joint Data Management Committee and investigators can use the data for evaluation of outcome of critical care, evaluation of medical resource, quality improvement, annual report, education and training, and critical care research.
Center of Outcome and Resource Evaluation (CORE) Adult Patient Database of Australian and New Zealand Intensive Care Society (ANZICS) was founded in 1992. More than 160 intensive care units in Australia and New Zealand contribute the data into this database. This database provides medical information to Australia and New Zealand government for critical care policy making and quality improvement. The primary aim of this proposal is to build a multicenter de-identification adult intensive care units database by mutual collaboration of multiple hospitals in Taiwan. This database will include the de-identification data accruing to the regulation of Health Insurance Portability and Accountability Act (HIPAA) of United States of America from each hospital. The data can be used to help the government and critical care societies evaluate the clinical outcomes of critical care. Furthermore, this data can help to effectively allocate the medical resource, improve quality, conduct multicenter registry-based clinical research, and publish high quality research. Hope to assist Taiwan and the world to improve critical care quality.
Study Overview
Detailed Description
The main purpose of this proposal is to build a multicenter de-identification adult intensive care units database in Taiwan. In future, the Joint Data Management Committee and investigators can use the data for evaluation of outcome of critical care, evaluation of medical resource, quality improvement, annual report, education and training, and critical care research.
Center of Outcome and Resource Evaluation (CORE) Adult Patient Database of Australian and New Zealand Intensive Care Society (ANZICS) was founded in 1992. More than 160 intensive care units in Australia and New Zealand contribute the data into this database. This database provides medical information to Australia and New Zealand government for critical care policy making and quality improvement. The primary aim of this proposal is to build a multicenter de-identification adult intensive care units database by mutual collaboration of multiple hospitals in Taiwan. This database will include the de-identification data accruing to the regulation of Health Insurance Portability and Accountability Act (HIPAA) of United States of America from each hospital. The data can be used to help the government and critical care societies evaluate the clinical outcomes of critical care. Furthermore, this data can help to effectively allocate the medical resource, improve quality, conduct multicenter registry-based clinical research, and publish high quality research. Hope to assist Taiwan and the world to improve critical care quality.
The Taiwan Society of Critical Care Medicine, Taiwan Society of Emergency and Critical Care Medicine, and National Taiwan University Hospital invite multiple hospitals to build the multicenter de-identification adult intensive care units database. This database includes only de-identification data. A Joint Data Management Committee will be organized and be in charge of data management. The data will be used for evaluation of outcome of critical care, evaluation of medical resource, quality improvement, and publication of mutual collaboration of critical care research in research ethic committee approved research filed.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Yu-Chang Yeh, MD, PhD
- Phone Number: +886-9-10513711
- Email: tonyyeh@ntuh.gov.tw
Study Locations
-
-
-
Kaohsiung, Taiwan
- Not yet recruiting
- Kaohsiung Medical University Hospital
-
Contact:
- Ming-Ju Tsai, MD, PhD
-
Kaohsiung, Taiwan
- Not yet recruiting
- Kaohsiung Veterans General Hospital
-
Contact:
- Wei-Chun Huang, MD, PhD
-
New Taipei, Taiwan
- Not yet recruiting
- Far Eastern Memorial Hospital
-
Contact:
- Hou-Tai Chang, MD
-
Taichung, Taiwan
- Recruiting
- Taichung Veteran General Hospital
-
Contact:
- Chieh-Liang Wu
-
Tainan, Taiwan
- Recruiting
- Chi Mei Medical Center
-
Contact:
- Chin-Ming Chen
-
Taipei, Taiwan
- Recruiting
- Mackay Memorial Hospital
-
Contact:
- Li-Kuo Kuo
-
Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Yu-Chang Yeh, MD, PhD
- Email: tonyyeh@ntuh.gov.tw
-
Taipei, Taiwan
- Not yet recruiting
- Taipei Medical University Hospital
-
Contact:
- An-Yi Wang
-
Taoyuan, Taiwan
- Not yet recruiting
- Chang Gung Medical Foundation
-
Contact:
- Kuan-Fu Chen, MD, PhD
-
Yun-Lin, Taiwan
- Not yet recruiting
- National Taiwan University Hospital Yun-Lin Branch
-
Contact:
- Chien-Hong Chou
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- •Critically ill patients admitted to intensive care units
Exclusion Criteria:
- •Critically ill patients admitted to intensive care units
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Critically ill patients
Patients received critical care in the intensive care units
|
Critical care in the intensive care units
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
30-day mortality
Time Frame: 30 days
|
mortality status at 30 days after admission to intensive care unit
|
30 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Length of stay in intensive care units
Time Frame: a median 2 to 7 days
|
Number of days in intensive care unite
|
a median 2 to 7 days
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- 202006006RINA
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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