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Clinical Trials/NCT02806492
NCT02806492
Completed
Not Applicable

Blood Pressure or Cardiac Output - the Influence on Cerebral Perfusion During Cardiopulmonary Bypass

UMC Utrecht1 site in 1 country15 target enrollmentJanuary 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cerebral Perfusion
Sponsor
UMC Utrecht
Enrollment
15
Locations
1
Primary Endpoint
regional cerebral oxygen saturation
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

The purpose of this study is to determine whether cerebral blood flow and cerebral tissue oxygenation is most dependent on cardiac output or on mean arterial pressure in patients undergoing cardiac surgery with the use of cardiopulmonary bypass.

Registry
clinicaltrials.gov
Start Date
January 2016
End Date
March 17, 2017
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Dr. B. van Zaane

MD PhD

UMC Utrecht

Eligibility Criteria

Inclusion Criteria

  • Undergoing cardiopulmonary bypass for CABG a
  • having an appropriate temporal bone window for reliable TCD monitoring
  • needing pharmacological intervention because of hypotension before going on CPB.

Exclusion Criteria

  • requiring hypothermia during surgery
  • requiring emergency surgery
  • contraindication for phenylephrine,
  • having known brain pathology (e.g. Cerebral Vascular Accident (CVA) or increased intracranial pressure
  • having a history of severe carotid artery stenosis.

Outcomes

Primary Outcomes

regional cerebral oxygen saturation

Time Frame: During surgery

mean velocity of blood flow of the middle cerebral artery

Time Frame: During surgery

Study Sites (1)

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