A Prospective Investigation of Pleth Variability Index (PVI) as a Dynamic Parameter of Fluid Responsiveness in Children
NCT ID: NCT02276599
Last Updated: 2018-10-18
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
9 participants
OBSERVATIONAL
2015-02-28
2018-05-31
Brief Summary
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Detailed Description
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Hypothesis: This study is designed to investigate the ability of PVI to non-invasively predict fluid responsiveness in mechanically ventilated children. The hypothesis is that a higher PVI will predict significant stroke volume increases in response to a fluid bolus in mechanically ventilated children.
Methods: The study population will consist of 20 children undergoing cardiac catheterization who will have normal (non-shunted) physiology at the conclusion of the procedure, ages 1-12 years. All subjects will receive a PVI measurement as well as a stroke volume measurement via transthoracic echocardiography. Subsequent volume expansion will be achieved with an intravenous bolus of 10 mL/kg of isotonic crystalloid (normal saline) administered over 10 minutes. After completion of the bolus, an additional PVI measurement and stroke volume measurement will be obtained.
Significance: Hypovolemia is a significant cause of harm in anesthetized and critically ill infants and children. In order to successfully resuscitate these patients, we must gain a better understanding of how to optimize cardiac output and oxygen delivery. A non-invasive monitor which indicates stroke volume responsiveness has the potential to better guide fluid resuscitation and improve outcomes.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Cardiac catheterization
Patients with a diagnosis of atrial septal defect who are having a cardiac catheterization.
Volume expansion
Fluid bolus of 0.9% normal saline 10 mL/kg over 10 minutes
Interventions
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Volume expansion
Fluid bolus of 0.9% normal saline 10 mL/kg over 10 minutes
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
1 Year
12 Years
ALL
No
Sponsors
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Brian Schloss
OTHER
Responsible Party
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Brian Schloss
Assistant Professor
Principal Investigators
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Brian Schloss, MD
Role: PRINCIPAL_INVESTIGATOR
Nationwide Children's Hospital
Locations
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Nationwide Children's Hospital
Columbus, Ohio, United States
Countries
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Other Identifiers
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IRB14-00332
Identifier Type: -
Identifier Source: org_study_id
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