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Clinical Trials/NCT03276364
NCT03276364
Completed
Not Applicable

The Impact of Point-of-Care Ultrasound Performed by Trainees to Improve the Prediction of Fluid Responsiveness in Patients With Shock

Montefiore Medical Center0 sites112 target enrollmentJuly 21, 2014
ConditionsUltrasoundShock

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Ultrasound
Sponsor
Montefiore Medical Center
Enrollment
112
Primary Endpoint
Fluid responsiveness
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Point-of-care ultrasound (POCUS) has been found to be useful for aiding in the prediction of fluid responsiveness. It is unknown if trainees can effectively utilize this tool to improve their assessment of fluid responsiveness.

In this prospective, observational study, pulmonary and critical care fellows are asked to make 2 assessments of fluid responsiveness in adults with shock: (1) based on clinical exam alone (Clinical) and (2) after performing a POCUS (Clinical + US). The accuracy of their pre- and post-ultrasound assessments are compared using a bioreactance monitor and passive leg raise test as the gold standard of fluid responsiveness in this study.

Registry
clinicaltrials.gov
Start Date
July 21, 2014
End Date
April 17, 2015
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Daniel G. Fein

Assistant Professor of Medicine

Montefiore Medical Center

Eligibility Criteria

Inclusion Criteria

  • Adults age 18 or older admitted to the MICU with a diagnosis of shock while a fellow was on duty.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Fluid responsiveness

Time Frame: Immediately subsequent to performance of a point-of-care ultrasound exam

Increase of stroke volume index greater than 10% following passive leg raise testing

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