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Clinical Trial Summary

The aim of this study is to assess the responsiveness of the standard minimally invasive hemodynamic monitors used in the operating room to known changes in the intravascular volume status that occur during blood removal and volume replacement with three different standard fluids used during ANH.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02179827
Study type Observational
Source University of California, Davis
Contact
Status Withdrawn
Phase
Start date November 2022
Completion date November 2024

See also
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