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Completed Phase 2 Interventional

Study Of An NK-1 Anti-Emetic Medication For The Prevention Of Post-Operative Nausea And Vomiting In Female Patients

ClinicalTrials.gov ID: NCT00600990

Public ClinicalTrials.gov record NCT00600990. 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 Sep 4, 2026, 1:39 PM EDT

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

Official title

Phase II Multicenter, Dose Ranging Study on the Safety and Antiemetic Efficacy of One Day Intraveous Dosing of GW597599 Administered With Ondansetron HCL in a Female Subjects Undergoing Surgical Procedures of High Emetogenic Risk

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the effectiveness of this medication in preventing nausea and vomiting in female patients at risk for post-operative nausea and vomiting (PONV).

Study identification

NCT ID
NCT00600990
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
624 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
Female
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
Nov 30, 2004
Primary completion
Jun 30, 2006
Completion
Jun 30, 2006
Last update posted
Jan 19, 2017

2004 – 2006

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205
GSK Investigational Site Glendale California 91206
GSK Investigational Site Laguna Hills California 95660
GSK Investigational Site Los Angeles California 90048
GSK Investigational Site Los Angeles California 90089
GSK Investigational Site Pasadena California 91109
GSK Investigational Site Boca Raton Florida 33067
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site Albany New York 12208
GSK Investigational Site New York New York 10021
GSK Investigational Site Durham North Carolina 27710
GSK Investigational Site Raleigh North Carolina 27609
GSK Investigational Site Philadelphia Pennsylvania 19141
GSK Investigational Site Dallas Texas 75390-9135
GSK Investigational Site Houston Texas 77024
GSK Investigational Site Spokane Washington 99204

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00600990, 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 Jan 19, 2017 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00600990 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →