Soluble Factors in the Serum of Severely Burned Patients
NCT ID: NCT02549079
Last Updated: 2015-09-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
23 participants
OBSERVATIONAL
2004-01-31
2008-12-31
Brief Summary
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Detailed Description
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Blood samples from severely burned patients will be collected over a period of five days and different cytokines (for example the macrophage migration inhibitory factor protein family) will be measured in the serum. Clinical data of the patients (sepsis, total body surface area of burns, abbreviated burn severity index, sepsis-related organ failure assessment, etc.) will be documented and correlated to the levels of soluble factors.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Blood sample
Blood will be taken from all patients meeting the inclusion criteria.
Eligibility Criteria
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Inclusion Criteria
* minimum of 10% total body surface area burn
* needing ICU treatment
Exclusion Criteria
* immunosuppression (e.g. HIV)
* undergone surgery 2 weeks prior to burn injury
* malignancies
* severe diseases (myocardial infarction, lung embolism)
* declining to participate in the study
18 Years
ALL
No
Sponsors
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RWTH Aachen University
OTHER
Responsible Party
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Principal Investigators
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Norbert Pallua, M.D., Ph.D.
Role: PRINCIPAL_INVESTIGATOR
RWTH Aachen University
Other Identifiers
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EK104/08
Identifier Type: -
Identifier Source: org_study_id
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