Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02625181 · ClinicalTrials.gov registry record · NA
Real-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis
A NA study, sponsored by Vanderbilt University.
- Completed
- Registry status
- NA
- Development phase
- 27,034
- Enrollment target
NCT02625181 is a NA study that has completed, run by Vanderbilt University. The registered enrollment target is 27,034 participants.
The verdict
NCT02625181, a NA study, has completed, sponsored by Vanderbilt University.
- COMPLETED
- Registry status
- NA
- Development phase
- 27,034 participants
- Enrollment target
Study Summary
The purpose of this study is to determine how automated recommendations are best presented to optimize the adherence to guidelines on prophylaxis for nausea and vomiting after surgery.
Interventions
- DEVICE Anesthesia Information Management System (AIMS)
- PROCEDURE Automated recommendation at the start of the case
- PROCEDURE Automated notification at the start of surgery
- PROCEDURE Preoperative recommendations: by email
- PROCEDURE Automated notification at the end of surgery
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 27,034 participants |
| Start Date | 2016-07 |
| Est. Completion | 2017-11-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02625181
The ClinicalTrials.gov registry entry for NCT02625181 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 27,034 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Anesthesia Information Management System (AIMS) is the first listed.
NCT02625181 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02625181 about?
NCT02625181 is a clinical study titled "Real-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis". The purpose of this study is to determine how automated recommendations are best presented to optimize the adherence to guidelines on prophylaxis for nausea and vomiting after surgery.
What is the current status of trial NCT02625181?
This trial is currently completed. It is a NA study. The enrollment target is 27,034 participants. The study started on 2016-07. Estimated completion is 2017-11-30.
What interventions are being tested in trial NCT02625181?
The interventions under investigation include: Anesthesia Information Management System (AIMS) (DEVICE), Automated recommendation at the start of the case (PROCEDURE), Automated notification at the start of surgery (PROCEDURE), Preoperative recommendations: by email (PROCEDURE), Automated notification at the end of surgery (PROCEDURE).
Who is sponsoring clinical trial NCT02625181?
This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.