Vasopressor SAT Study
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Critical Illness
- Delirium
- Low Blood Pressure
- Type
- Observational
- Design
- Observational Model: CohortTime Perspective: Prospective
Participation Requirements
- Age
- Between 18 years and 125 years
- Gender
- Both males and females
Description
This observational study will compare mean arterial pressure and vasoactive drug dose recorded at two time points: prior to awakening from sedation during the awakening from sedation trial The vasoactive infusion will be titrated to a mean arterial pressure as determined by the medical team prior to...
This observational study will compare mean arterial pressure and vasoactive drug dose recorded at two time points: prior to awakening from sedation during the awakening from sedation trial The vasoactive infusion will be titrated to a mean arterial pressure as determined by the medical team prior to study enrollment. Each enrolled patient will have measurements taken only on the first day of enrollment. Enrolled subjects will also have a delirium assessment using the CAM-ICU tool before the awakening from sedation trial and during the awakening from sedation trial.
Tracking Information
- NCT #
- NCT03182335
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: John Kress, MD University of Chicago
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