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Clinical Trials/NCT00469716
NCT00469716
Completed
Phase 4

Infusion of Hypertonic Saline-hetastarch in Cardiac Surgery

Haukeland University Hospital1 site in 1 country50 target enrollmentApril 2007

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Postoperative Cardiorespiratory Failure
Sponsor
Haukeland University Hospital
Enrollment
50
Locations
1
Primary Endpoint
Cardiac output, intrathoracic blood volume, extravascular lung water, global enddiastolic volume
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Cardiopulmonary bypass(CPB) is associated with increased fluid extravasation and edema formation. A continuous infusion of a mixture of hypertonic saline/hydroxyethyl starch (HSH)during CPB reduced fluid extravasation and total fluid gain during bypass in an animal model. We hypothesize that a continuous infusion of HSH will reduce fluid load and increase hemodynamic and respiratory functions in patients undergoing coronary artery bypass with CPB.

Detailed Description

Cardiopulmonary bypass (CPB) is associated with fluid overload and edema formation occasionally resulting in vital organ dysfunction affecting heart, respiratory system , gastrointestinal tract and brain. Hyperosmolar/hyperoncotic preparations (HSH/HSD) have been used in cardiac surgery essentially with the aim to mobilize fluid excess and improve postoperative cardiorespiratory function.Most studies dealing with the administration of HSD or HSH during and after CPB, have used protocols recommended for treatment of severe hypovolemia and shock, that is 4 mL/kg as a bolus, given within minutes.In animal experiments we have used HSD or HSH, 1 mL/kg/h to a total dose of 4 mL/kg during CPB. The use of HSH/HSD reduced the total fluid gain about 50 % and resulted in significantly lower content of tissue water in vital organs as heart and lungs. In the actual clinical trial we hypothesize that a continuous infusion of HSH will reduce fluid load and increase hemodynamic and respiratory functions monitored with the PiCCO system in patients undergoing coronary artery bypass with CPB.

Registry
clinicaltrials.gov
Start Date
April 2007
End Date
May 2008
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Haukeland University Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients scheduled for elective coronary artery bypass graft surgery

Exclusion Criteria

  • Age \<18 years or \> 75 years
  • BMI\< 18 or \> 30
  • Left ventricular ejection fraction \< 40%
  • Emergency operations
  • Additional valvular diseases
  • Impaired renal function
  • Serum sodium\> 145 mmol/l
  • Hematocrit\< 30%
  • Use of clopidogrel the last 5 days

Outcomes

Primary Outcomes

Cardiac output, intrathoracic blood volume, extravascular lung water, global enddiastolic volume

Time Frame: 12 hours

Secondary Outcomes

  • Time to extubation, fluid balance, paO2/FiO2- ratio, frequency of atrial fibrillation, cytokines, time to ICU-release and hospital release.

Study Sites (1)

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