Real-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis

Completed · Not applicable

Conditions studied: Postoperative Nausea and Vomiting

In brief

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.

Key facts

Study ID

NCT02625181

Run by

Vanderbilt University

People needed

27034

Starts

2016-07-01

Expected to finish

2017-11-30

Last updated by the study team

2019-03-07

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• All adult patients (18 years and older) that are scheduled for an elective surgical procedure under general anesthesia

You may not qualify if…

• Patients undergoing emergency surgery or organ transplantation
• Patients that are transferred directly to the Intensive Care Unit after the end of the procedure
• Patients that die intraoperatively
• Procedures that only require a sedative level of anesthesia

Where it is running

• Vanderbilt University Medical Center — Nashville, Tennessee, United States

Full record on ClinicalTrials.gov

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