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Sponsored by: |
Danish Procalcitonin Study Group |
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Information provided by: | Danish Procalcitonin Study Group |
ClinicalTrials.gov Identifier: | NCT00144638 |
Procalcitonin, a marker of infection has often been compared to clinical pictures as for instance "clinical sepsis". This has given som problems in the interpretation of these studies, because of the lack of good Gold Standards for "clinical sepsis. We have decided to investigate the development from day to day of Procalcitonin in the blood of intensive care patients, compared to the mortality.
Hypothesis: Procalcitonin increase after reaching a certain level predicts mortality in the Intensive Care Unit.
Condition |
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Sepsis - to Reduce Mortality in the Intensive Care Unit |
Study Type: | Observational |
Study Design: | Natural History, Longitudinal, Defined Population, Prospective Study |
Official Title: | Procalcitonin Increase Identifies Critically Ill Patients at High Risk of Mortality |
Estimated Enrollment: | 450 |
Study Start Date: | January 2002 |
Estimated Study Completion Date: | January 2003 |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria: Admitted to the ICU 4131 of Rigshospitalet Copenhagen University Hospital in the year 2002
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Exclusion Criteria:
Recent (< 3 months) liver transplantation
Expected admission < 24 h
Denmark | |
Dept. 4131, Rigshospitalet, Cph University Hosp., DK | |
Copenhagen, Denmark, DK-2100 |
Principal Investigator: | Lars Heslet, MD, MD.Sc. | Dept. 4131, Rigshospitalet, Blegdamsvej 9, DK-2100 |
Study ID Numbers: | DPSG1 |
Study First Received: | September 1, 2005 |
Last Updated: | September 1, 2005 |
ClinicalTrials.gov Identifier: | NCT00144638 |
Health Authority: | Denmark: National Board of Health |
Sepsis Critical Illness |
Disease Attributes Pathologic Processes |