Caretaker vs. Blood Pressure Monitoring With Invasive Arterial Pressure Monitoring in Patients With Septic Shock
NCT ID: NCT03933722
Last Updated: 2024-02-07
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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ACTIVE_NOT_RECRUITING
40 participants
OBSERVATIONAL
2019-02-04
2024-02-05
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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Caretaker
Comparing blood pressure obtained using routine blood pressure sphygmomanometer to a non-invasive device that continuously monitors central blood pressure (CareTaker).
Caretaker
Application of Caretaker device to subjects that have septic shock and that have an invasive arterial pressure monitor placed.
Interventions
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Caretaker
Application of Caretaker device to subjects that have septic shock and that have an invasive arterial pressure monitor placed.
Eligibility Criteria
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Inclusion Criteria
* Greater than or equal to 18 years of age.
* Have an arterial catheter already in place.
Exclusion Criteria
* Contraindication to the application of the Caretaker device due to pre-existing finger injury.
* Patients in whom use of a BP cuff is contraindicated.
18 Years
ALL
No
Sponsors
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The Cooper Health System
OTHER
Responsible Party
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Principal Investigators
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Irwin Gratz, MD
Role: PRINCIPAL_INVESTIGATOR
The Cooper Health System
Locations
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Cooper University Hospital
Camden, New Jersey, United States
Countries
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Other Identifiers
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18-180EX
Identifier Type: -
Identifier Source: org_study_id
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