CompletedN/Aketamine
Real-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis
Sponsored by Vanderbilt University
NCT ID
NCT02625181
Target Enrollment
27,034 participants
Start Date
2016-07
Est. Completion
2017-11-30
About This Study
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.
Conditions Studied
Interventions
- •Automated recommendation at the start of the case
- •Automated notification at the start of surgery
- •Preoperative recommendations: by email
- •Automated notification at the end of surgery
- •Anesthesia Information Management System (AIMS)
- •Perioperative Data Warehouse (PDW)
- •General anesthesia
- •Elective surgery
- •Propofol
- •Sevoflurane
- •Isoflurane
- •Desflurane
- •Scopolamine
- •Droperidol
- •Haloperidol
- •Dexamethasone
- •Promethazine
- •Meclizine
- •Aprepitant
- •Metoclopramide
- •Fentanyl
- •Sufentanil
- •Alfentanil
- •Remifentanil
- •Morphine
- •Meperidine
- •Hydromorphone
- •Methadone
- •Oxycodone
- •Oxymorphone
- •Hydrocodone
- •Ketamine
- •Ondansetron
- •Granisetron
- •Dolasetron mesylate
- •Palonosetron
- •Tropisetron
- •Ramosetron
Eligibility
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria: * All adult patients (18 years and older) that are scheduled for an elective surgical procedure under general anesthesia Exclusion Criteria: * 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
Study Locations (1)
Vanderbilt University Medical Center
Nashville, Tennessee, United States