Taiwan Center of Outcome and Resource Evaluation

February 18, 2024 updated by: National Taiwan University Hospital

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

Status

Recruiting

Conditions

Intervention / Treatment

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

Observational

Enrollment (Estimated)

600000

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

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:
      • 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

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

Sampling Method

Non-Probability Sample

Study Population

Critically ill patients admitted to intensive care units

Description

Inclusion Criteria:

  • •Critically ill patients admitted to intensive care units

Exclusion Criteria:

  • •Critically ill patients admitted to intensive care units

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

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

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)

April 1, 2022

Primary Completion (Estimated)

July 1, 2040

Study Completion (Estimated)

December 1, 2040

Study Registration Dates

First Submitted

May 3, 2021

First Submitted That Met QC Criteria

May 3, 2021

First Posted (Actual)

May 6, 2021

Study Record Updates

Last Update Posted (Actual)

February 20, 2024

Last Update Submitted That Met QC Criteria

February 18, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 202006006RINA

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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