Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional

Casopitant (Oral) And ZOFRAN To Prevent Postoperative Nausea And Vomiting In Women

ClinicalTrials.gov ID: NCT00326248

Public ClinicalTrials.gov record NCT00326248. 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 24, 2026, 5:54 AM EDT

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

Official title

A Phase III, Multicenter, Randomized, Double-blind, Parallel Group Study to Evaluate the Safety and Efficacy of 50mg Oral Dosing With the Neurokinin-1 Receptor Antagonist GW679769 for the Prevention of Postoperative Nausea and Vomiting in Female Subjects at High Risk for Emesis

Study identification

NCT ID
NCT00326248
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
482 participants

Conditions and interventions

Interventions

  • GW679769 (casopitant) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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
Feb 28, 2006
Primary completion
Jun 30, 2006
Completion
Jun 30, 2006
Last update posted
Oct 25, 2016

2006

United States locations

U.S. sites
26
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
GSK Investigational Site Montgomery Alabama 36106
GSK Investigational Site Sheffield Alabama 35660
GSK Investigational Site Phoenix Arizona 85032
GSK Investigational Site Los Angeles California 90033
GSK Investigational Site Boynton Beach Florida 33437
GSK Investigational Site Jacksonville Florida 32216
GSK Investigational Site Melbourne Florida 32901
GSK Investigational Site Miami Florida 33136
GSK Investigational Site Naples Florida 34108
GSK Investigational Site Pensacola Florida 32504
GSK Investigational Site Anderson Indiana 46011
GSK Investigational Site Grand Rapids Michigan 49503
GSK Investigational Site Jackson Mississippi 39202
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site New Brunswick New Jersey 08901
GSK Investigational Site New Brunswick New Jersey 8903
GSK Investigational Site New York New York 10016
GSK Investigational Site New York New York 10025
GSK Investigational Site The Bronx New York 10467
GSK Investigational Site Altoona Pennsylvania 16602
GSK Investigational Site Philadelphia Pennsylvania 19102
GSK Investigational Site Pittsburgh Pennsylvania 15213
GSK Investigational Site Pittsburgh Pennsylvania 15232
GSK Investigational Site Houston Texas 77030
GSK Investigational Site San Antonio Texas 78240
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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00326248, 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 Oct 25, 2016 · Synced Jul 24, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00326248 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →