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Fluid Investigation Colloid vs Crystalloid Reg. Renal Hemodynamics and Function

S

Sahlgrenska University Hospital

Status

Completed

Conditions

Renal Impairment

Treatments

Drug: colloid
Drug: crystalloid

Study type

Interventional

Funder types

Other

Identifiers

NCT01729364
vätskestudien

Details and patient eligibility

About

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

Full 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.

Enrollment

30 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • elective fast track CABG patients, postoperative

Exclusion criteria

  • hemodynamic instability
  • preoperative renal impairment
  • major postoperative bleeding

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

crystalloid
Experimental group
Description:
crystalloid fluid administration, Ringer-acetat 20ml/kg under 30 minutes
Treatment:
Drug: crystalloid
colloid
Experimental group
Description:
colloidal fluids administration, HES 6% (130/0,4) 7ml/kg under 30 minutes
Treatment:
Drug: colloid

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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