Fluid Responsiveness Prediction at the Bedside

NCT00721604 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2009-08-03

No results posted yet for this study

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

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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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00721604 on ClinicalTrials.gov