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NCT06117605 · ClinicalTrials.gov registry record · NA
Sepsis Electronic Prompting for Timely Intervention and Care for Emergency Department Patients
A NA study of Sepsis and Electronic Health Records, sponsored by Columbia University.
- Completed
- Registry status
- NA
- Development phase
- 25,668
- Enrollment target
- 1
- Study location
NCT06117605 is a NA study of Sepsis and Electronic Health Records that has completed, run by Columbia University. The registered enrollment target is 25,668 participants, above the 6,279-participant average among 90 other Sepsis trials with a reported enrollment target (309% higher). The trial reports 1 study location across 1 state.
The verdict
NCT06117605, a NA study of Sepsis and Electronic Health Records, has completed, sponsored by Columbia University.
- COMPLETED
- Registry status
- NA
- Development phase
- 25,668 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to study systemic inflammatory response syndrome (SIRS) electronic health record (EHR) alerts for sepsis in the emergency department (ED). The main question it aims to answer is: do nurse alerts, prescribing clinician alerts, or both nurse and prescribing clinician alerts improve time to sepsis treatment for patients in the ED? Nurses and prescribing clinicians will receive SIRS alerts based on the group to which the patient is randomly assigned. Researchers will compare four groups: no alerts, nurse alerts only, prescribing clinician alerts only, or both nurse and prescribing clinician alerts.
Conditions Studied
Interventions
- OTHER Nurse SIRS alert
- OTHER Prescribing clinician SIRS alert
Study Locations (1)
New York
- NewYork-Presbyterian Hospitals - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25,668 participants |
| Start Date | 2023-11-14 |
| Est. Completion | 2024-07-22 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06117605
The ClinicalTrials.gov registry entry for NCT06117605 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 25,668 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 6,279-participant average among 90 other Sepsis trials with a reported enrollment target (309% higher). The listed sponsor is Columbia University, which has 958 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Sepsis appearing as the primary indexed condition, and to 2 interventions - of which Nurse SIRS alert is the first listed.
NCT06117605 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT06117605 about?
NCT06117605 is a clinical study titled "Sepsis Electronic Prompting for Timely Intervention and Care for Emergency Department Patients". The goal of this clinical trial is to study systemic inflammatory response syndrome (SIRS) electronic health record (EHR) alerts for sepsis in the emergency department (ED). The main question it aims to answer is: do nurse alerts, prescribing clinician alerts, or both nurse and prescribing clinician...
What is the current status of trial NCT06117605?
This trial is currently completed. It is a NA study. The enrollment target is 25,668 participants. The study started on 2023-11-14. Estimated completion is 2024-07-22.
What conditions does trial NCT06117605 study?
This clinical trial studies the following conditions: Sepsis, Electronic Health Records, Clinical Decision Support Systems.
What interventions are being tested in trial NCT06117605?
The interventions under investigation include: Nurse SIRS alert (OTHER), Prescribing clinician SIRS alert (OTHER).
Who is sponsoring clinical trial NCT06117605?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06117605 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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