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Neuroaxial Blokade and Blood Pressure

Hypovolemia Clinical Trial

Official title:
Neuroaxial Blokade and the Effect of Fluid Optimization

Clinical Trial Summary

The effect of individualized fluid optimization during neuroaxial blockade has not been evaluated. The investigators evaluated if if Stroke decrease 15 min after activation of neuroaxial blockade and whether SV could be optimized to pre activation values.

Clinical Trial Description

The purpose of this study is to evaluate SV maximization with aid of the LiDCO system which is a minimal invasive technique only requiring a venous and arterial line. We thereby attempt to cover the specific individual fluid deficit induced by neuroaxial blockade. ;

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00435422
Study type Interventional
Source Rigshospitalet, Denmark
Contact Morten Bundgaard-Nielsen, MD
Phone 0045 35 45 09 55
Email morten.bundgaard-nielsen@rh.dk
Status Recruiting
Phase N/A
Start date January 2010
Completion date May 2010
View Details
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