About this trial

The purpose of this study is evaluate goal-directed therapy with continuous central venous saturation compared to standard therapy in children undergoing cardiac surgery.

Eligibility criteria

Qualifiers

Elective cardiac surgery with cardiopulmonary bypass

Written informed consent

Disqualifiers

Cardiac arrhythmia

Emergency operation

Hemodynamic instabillty (norepinephrine higher than 1 mcg/kg/min)

Neoplasia

Trial design

Treatments tested in this trial

  • Continuous central venous oxygenation monitoring
  • Standard protocol

Treatment groups

65 Participants
are divided into 2 treatment groups

Locations

1
Incor - Heart Institute - University of Sao Paulo05403000, São Paulo Brazil

Sponsors and collaborators

Instituto do Coracao

Lead sponsor