Expired Study
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St. Louis, Missouri 63110


Purpose:

The short term goal of this study is to evaluate a non-invasive approach that optimizes intravenous (IV) fluid administration according to heart performance and results in surrogate improvements in morbidity and mortality via lactate clearance. Additional objectives include comparative assessments of methods for determining volume responsiveness and establishing a prevalence of volume responsive shock in the Emergency Department (ED).


Criteria:

Inclusion Criteria: - Hypotension (Systolic Blood Pressure ≤90mm Hg or Mean Arterial Pressure ≤ 65 mm Hg) after ≥ 20ml/kg fluids OR - Vasopressor Use OR - Lactate ≥ 2.5 mmol/L Exclusion Criteria: - Pulse Oximetry <90% despite supplemental oxygen or intubation - Seizure in the last 24 hours - Prisoner - Pregnancy - Age <18 - Allergy to coupling or ultrasound gel - Inability to do passive leg raise - Inability to obtain IV access - Treating clinician discretion


NCT ID:

NCT01128413


Primary Contact:

Principal Investigator
Christopher V Holthaus, MD
Washington University School of Medicine


Backup Contact:

N/A


Location Contact:

St. Louis, Missouri 63110
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: August 31, 2019

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