Status:

UNKNOWN

Neuroaxial Blokade and Blood Pressure

Lead Sponsor:

Rigshospitalet, Denmark

Conditions:

Hypovolemia

Eligibility:

All Genders

18-80 years

Phase:

NA

Brief 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 ...

Detailed 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 s...

Eligibility Criteria

Inclusion

  • Neuroaxial blockade (thoracic)

Exclusion

  • Weight below 40 kg
  • Lithium therapy
  • Type I diabetes or type II requiring insulin

Key Trial Info

Start Date :

January 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

May 1 2010

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT00435422

Start Date

January 1 2010

End Date

May 1 2010

Last Update

March 25 2010

Active Locations (1)

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1

Rigshospitalet

Copenhagen, Denmark, 2100