Clinical Trials Directory

Trials / Completed

CompletedNCT01827007

Assessment of Fluid Responsiveness by Elevation of PEEP in Patients With Septic Shock

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Helsinki University Central Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The aim of the study is to evaluate whether fluid responsiveness of the critically ill patient can be assessed by analysing the PEEP-induced hemodynamic effects to systolic blood pressure, pulse pressure, aortic blood flow, aortic time-velocity integral and left ventricular end diastolic area measured with transesophageal echocardiography (PEEP-test). The chances are compared to increase of CI after volume expansion (gold standard). In clinical practise, it would be especially relevant if PEEP-induced changes in arterial pressure variations could be used in evaluation of volume status and fluid responsiveness. However, as ECHO-derived variables are used in greater extent to guide the treatment with inappropriate evidence, the simultaneous registration of ECHO-derived hemodynamic measurements is essential in the study design.

Conditions

Interventions

TypeNameDescription
OTHERVolume expansion with gelofusine

Timeline

Start date
2008-01-01
Primary completion
2012-12-01
Completion
2013-02-01
First posted
2013-04-09
Last updated
2013-04-09

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT01827007. Inclusion in this directory is not an endorsement.