Clinical Trials Directory

Trials / Completed

CompletedNCT01729364

Fluid Investigation Colloid vs Crystalloid Reg. Renal Hemodynamics and Function

Colloid vs Crystalloid Infusion Postoperative in CABG Patients Regarding Renal Hemodynamics and Function

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Sahlgrenska University Hospital · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Comparing the effects of crystalloid versus colloid fluid resuscitation in CABG patients postoperatively regarding renal blood flow, glomerular filtration rate and renal oxygen demand.

Detailed description

Due to blood loss and SIRS postoperative hypovolemia is a usual feature after CABG surgery. Substantial controversy persists regarding the best choice of fluid to be used for resuscitation in this setting regarding renal function and oxygen supply-demand matching. In our study we aim to investigate differences in functional renal parameters by dividing patients postoperatively in two groups, substituted either with crystalloid fluid, Ringer-Acetat, 20 ml/kg or colloid, HES 6% (130/0,4) 10 ml/kg under 20 minutes. Central and renal hemodynamics will be measured before (baseline) and after fluid administration by blood sampling and thermodilution in both pulmonary artery catheter and renal vein catheter. Measurement endpoints will mainly consist of central hemodynamics, renal blood flow, GFR and renal oxygen extraction rate which we aim to compare between groups.

Conditions

Interventions

TypeNameDescription
DRUGcrystalloid
DRUGcolloid

Timeline

Start date
2008-04-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2012-11-20
Last updated
2015-05-22

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT01729364. Inclusion in this directory is not an endorsement.