The Use of the USCOM Device in Addition to Cardiac Ultrasound in Patients Undergoing Treatment for Undifferentiated Shock
NCT ID: NCT01981629
Last Updated: 2014-10-24
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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COMPLETED
47 participants
OBSERVATIONAL
2012-07-31
2013-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Shock
Defined by systolic blood pressure less than 95 mmHg or shock index (heart rate/systolic blood pressure) greater than 0.9
USCOM
The USCOM device will be used in addition to cardiac ultrasound in patients with shock.
Interventions
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USCOM
The USCOM device will be used in addition to cardiac ultrasound in patients with shock.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Pregnant
* Patients in shock due to trauma
18 Years
ALL
No
Sponsors
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Hennepin Healthcare Research Institute
OTHER
Responsible Party
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Principal Investigators
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Johanna C Moore, MD
Role: PRINCIPAL_INVESTIGATOR
Hennepin Healthcare Research Institute
Locations
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Hennepin County Medical Center
Minneapolis, Minnesota, United States
Countries
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Other Identifiers
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12-3496
Identifier Type: -
Identifier Source: org_study_id
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