At a glance
ClinicalIndex Comparison RecordN/ACompleted· 51 enrolled
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
NT-proBNP in Postoperative/Posttraumatic Critically Ill Patients With Severe SIRS/Sepsis and Shock
In Brief
An observational study for SIRS and 4 related conditions. Completed, enrolled 51 participants across 1 site.
Detailed Summary
The purpose of this study is to determine the course of NT-proBNP plasma concentrations in the context of confounding parameters in postoperative/posttraumatic critically ill patients with severe SIRS/sepsis and shock.
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsSIRS, Sepsis, Shock, Critically Ill, Multiple Organ Dysfunction Syndrome
CountriesGermany
Collaborators--
Timeline
N/ACompletedFinished
2009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartAug 2008
First PostedAug 2008
Primary CompletionAug 2012
Study CompletionDec 2012
TodayJul 2026
First PostedAug 18, 2008
Enrollment StartAug 1, 2008
Primary CompletionAug 1, 2012
Study CompletionDec 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4 yearsPosted 17.9 years ago