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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 March 2015 |
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Main ID: |
NCT02367768 |
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Date of registration:
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06/02/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Long-term Outcome Related Prognostic Factor and Biomarkers of Major Trauma Database Analysis
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Scientific title:
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Long-term Outcome Related Prognostic Factor and Biomarkers of Major Trauma Database Analysis |
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Date of first enrolment:
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February 2015 |
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Target sample size:
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500 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT02367768 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Prospective
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Phase:
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N/A
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Countries of recruitment
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Taiwan
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Contacts
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Name:
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Ying-Ru Chen, Master |
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Address:
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Telephone:
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886972651471 |
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Email:
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ronaldinhol@hotmail.com |
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Affiliation:
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Name:
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Ting-Chun Kuo, M.D. |
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Address:
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Telephone:
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Email:
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Affiliation:
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No.7, Chung San South Road, Taipei City 100, Taiwan (R.O.C.) |
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Name:
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Ting-Chun Kuo |
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Address:
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Telephone:
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886-97265-3245 |
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Email:
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tina@ntuh.gov.tw |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria:
- age ? 20
- willing to join this study and sign the inform consent form by the patients or their
contactable families
- ISS score ? 16, or meet trauma blue or trauma red criteria
- response to primary resuscitation
- without uncontrolled or major (>1500mL) bleeding.
Exclusion criteria:
- active malignancy before the event of major trauma
- age <20, pregnancy woman, breast-feeding woman, or mental illness
- uncontrolled bleeding with hemoglobin <7g/dL after treatment.
Age minimum:
20 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Wounds and Injuries
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Primary Outcome(s)
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Event related survival
[Time Frame: 30 days]
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Secondary Outcome(s)
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Functional status
[Time Frame: 12 months]
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over all survival
[Time Frame: 2 years]
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Secondary ID(s)
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201410060RINA
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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