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Completed Phase 3 Interventional

Casopitant And ZOFRAN To Prevent Post Operative Nausea And Vomiting In Women

ClinicalTrials.gov ID: NCT00334152

Public ClinicalTrials.gov record NCT00334152. 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 Oct 21, 2026, 4:07 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 the 30 mg Intravenous Formulation of the Neurokinin-1 Receptor Antagonist GW679769 for Prevention of Postoperative Nausea and Vomiting in Female Subjects at High Risk for Emesis

Brief summary

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

This study is being conducted to see if adding GW679769 (casopitant) to ZOFRAN will significantly decrease the number of patients who experience nausea and vomiting after surgery.

Study identification

NCT ID
NCT00334152
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
515 participants

Conditions and interventions

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
Mar 2006 (Type not available)
Primary completion
Jul 2006 (Actual)
Completion
Jul 2006 (Actual)
Last update posted
Mar 23, 2017

2006

United States locations

U.S. sites
25
U.S. states
14
U.S. cities
25
Facility City State ZIP Site status
GSK Investigational Site Fairhope Alabama 36532 —
GSK Investigational Site Mobile Alabama 36608 —
GSK Investigational Site Montgomery Alabama 36106 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Arcadia California 91007 —
GSK Investigational Site Glendale California 91206 —
GSK Investigational Site Laguna Hills California 92653 —
GSK Investigational Site Pasadena California 91105 —
GSK Investigational Site Boca Raton Florida 33067 —
GSK Investigational Site Melbourne Florida 32901 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site West Palm Beach Florida 33409 —
GSK Investigational Site Chicago Illinois 60637 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Baltimore Maryland 21229-5299 —
GSK Investigational Site Royal Oak Michigan 48073 —
GSK Investigational Site Mineola New York 11501 —
GSK Investigational Site New Hyde Park New York 11040 —
GSK Investigational Site New York New York 10038 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Cincinnati Ohio 45208 —
GSK Investigational Site Oklahoma City Oklahoma 73104 —
GSK Investigational Site Charlottesville Virginia 22908 —
GSK Investigational Site Winchester Virginia 22601 —
GSK Investigational Site Seattle Washington 98195 —

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00334152, 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 23, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00334152 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →