Overview

Fenoldopam and Splanchnic Perfusion During Cardiopulmonary Bypass

Status:
Completed
Trial end date:
2009-04-01
Target enrollment:
0
Participant gender:
All
Summary
Cardiopulmonary bypass (CPB) for cardiac operations may be accompanied by different patterns of visceral underperfusion. This could result in clinical patterns of lactic acidosis but in the most severe cases there is the risk for mesenteric infarction (0.2% of the cases). Renal function as well may be impaired due to a low oxygen delivery, and acute renal failure occurs in 1-2% of cases. Fenoldopam mesilate is a selective splanchnic vasodilator when used at a dose < 0.1 mcg/kg/min. The experimental hypothesis of this randomized, controlled trial (RCT) is that the use of fenoldopam may determine a better visceral perfusion during CPB.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
IRCCS Policlinico S. Donato
Treatments:
Fenoldopam
Criteria
Inclusion Criteria:

- Complex, combined cardiac operation

- Predicted CPB duration > 90 minutes

Exclusion Criteria:

- Age < 18 years

- No written informed consent