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Completed Not applicable Interventional Results available

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

ClinicalTrials.gov ID: NCT02625181

Public ClinicalTrials.gov record NCT02625181. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 7:43 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT02625181
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Vanderbilt University
Other
Enrollment
27,034 participants

Conditions and interventions

Interventions

  • 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
  • Anesthesia Information Management System (AIMS) Device
  • Perioperative Data Warehouse (PDW) Device
  • General anesthesia Procedure
  • Elective surgery Procedure
  • Propofol Drug
  • Sevoflurane Drug
  • Isoflurane Drug
  • Desflurane Drug
  • Scopolamine Drug
  • Droperidol Drug
  • Haloperidol Drug
  • Dexamethasone Drug
  • Promethazine Drug
  • Meclizine Drug
  • Aprepitant Drug
  • Metoclopramide Drug
  • Fentanyl Drug
  • Sufentanil Drug
  • Alfentanil Drug
  • Remifentanil Drug
  • Morphine Drug
  • Meperidine Drug
  • Hydromorphone Drug
  • Methadone Drug
  • Oxycodone Drug
  • Oxymorphone Drug
  • Hydrocodone Drug
  • Ketamine Drug
  • Ondansetron Drug
  • Granisetron Drug
  • Dolasetron mesylate Drug
  • Palonosetron Drug
  • Tropisetron Drug
  • Ramosetron Drug

Procedure · Device · Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 30, 2016
Primary completion
Nov 1, 2017
Completion
Nov 29, 2017
Last update posted
Mar 6, 2019

2016 – 2017

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Vanderbilt University Medical Center Nashville Tennessee 37212

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02625181, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 6, 2019 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02625181 live on ClinicalTrials.gov.

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