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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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19 February 2015 |
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Main ID: |
NCT01503684 |
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Date of registration:
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02/01/2012 |
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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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Biomarkers in Exhaled Breath Condensates of Septic Patients to Predict Development of Multi-organ Dysfunction Syndrome
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Scientific title:
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Biomarkers in Exhaled Breath Condensates of Septic Patients to Predict Development of Multi-organ Dysfunction Syndrome |
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Date of first enrolment:
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August 2011 |
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Target sample size:
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300 |
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Recruitment status: |
Recruiting |
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URL:
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http://clinicaltrials.gov/show/NCT01503684 |
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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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Jih-Shuin Jerng, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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National Taiwan University Hospital |
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Name:
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Jih-Shuin Jerng, MD,PhD |
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Address:
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Telephone:
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886-2-23562905 |
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Email:
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jsjerng@ntu.edu.tw |
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Affiliation:
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Name:
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Jih-Shuin Jerng, MD, PhD |
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Address:
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Telephone:
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886-2-23562905 |
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Email:
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jsjerng@ntu.edu.tw |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- above 20 years old
- admitted to ICU with the diagnosis of sepsis and treated with mechanical ventilation
via an endotracheal tube
Exclusion Criteria:
- pregnant
- active malignancy
- in an immunosuppressed status such as HIV disease, neutropenia, being treated with
immunosuppressive agents
- expected to have an unavoidable very short life expectancy after admission, i.e., < 3
days
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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Sepsis
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Intervention(s)
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Other: Determined by intended physician
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Primary Outcome(s)
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Development and severity of sepsis
[Time Frame: 28 days]
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Secondary Outcome(s)
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Response to treatment and progression of organ failure
[Time Frame: 28 days]
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Mortality
[Time Frame: 28 days]
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Secondary ID(s)
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201106068RC
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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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