Fluid Responsiveness Prediction at the Bedside
NCT00721604 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2009-08-03
Summary
The purpose of this study is to verify the accuracy and applicability of predictors of fluid administration efficacy in hypotensive critically ill patients.
Conditions
- Hypotension
- Shock
Interventions
- DRUG
-
fluid administration
two consecutive infusions of 6% hydroxyethyl starch at the dosage 7 ml/kg over 30 minutes (total 14 ml/kg in 60 minutes)
Sponsors & Collaborators
-
Fondazione Poliambulanza Istituto Ospedaliero
lead OTHER
Principal Investigators
-
Giuseppe Natalini, MD · Fondazione Poliambulanza Istituto Ospedaliero
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2008-07-31
- Primary Completion
- 2009-04-30
- Completion
- 2009-05-31
Countries
- Italy
Study Locations
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