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NCT03182335 · ClinicalTrials.gov registry record
Vasopressor SAT Study
A clinical trial of Critical Illness and Delirium, sponsored by University of Chicago.
- Active
- Registry status
- 800
- Enrollment target
- 1
- Study location
NCT03182335 is a study of Critical Illness and Delirium that is active but no longer recruiting, run by University of Chicago. The registered enrollment target is 800 participants, below the 3,130-participant average among 91 other Critical Illness trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03182335, a study of Critical Illness and Delirium, is active but no longer recruiting, sponsored by University of Chicago.
- ACTIVE NOT RECRUITING
- Registry status
- 800 participants
- Enrollment target
- 1
- Study location
Study Summary
To assess the impact of daily awakening from sedation on the amount of vasoactive medication required in the ICU. The hypothesis of this proposal is that the amount of vasoactive drug required to maintain an adequate mean arterial blood pressure will be reduced during a daily awakening from sedation.
Conditions Studied
Interventions
- OTHER sedation awakening trial
Study Locations (1)
Illinois
- The University of Chicago Medical Center - Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 800 participants |
| Start Date | 2014-04-28 |
| Est. Completion | 2026-06 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03182335
The ClinicalTrials.gov registry entry for NCT03182335 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 800 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,130-participant average among 91 other Critical Illness trials with a reported enrollment target (74% lower). The listed sponsor is University of Chicago, which has 796 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Critical Illness appearing as the primary indexed condition, and to 1 intervention - of which sedation awakening trial is the first listed.
NCT03182335 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT03182335 about?
NCT03182335 is a clinical study titled "Vasopressor SAT Study". To assess the impact of daily awakening from sedation on the amount of vasoactive medication required in the ICU. The hypothesis of this proposal is that the amount of vasoactive drug required to maintain an adequate mean arterial blood pressure will be reduced during a daily awakening from sedation...
What is the current status of trial NCT03182335?
This trial is currently active not recruiting. The enrollment target is 800 participants. The study started on 2014-04-28. Estimated completion is 2026-06.
What conditions does trial NCT03182335 study?
This clinical trial studies the following conditions: Critical Illness, Delirium, Low Blood Pressure.
What interventions are being tested in trial NCT03182335?
The interventions under investigation include: sedation awakening trial (OTHER).
Who is sponsoring clinical trial NCT03182335?
This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03182335 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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