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Casopitant (Oral) And ZOFRAN To Prevent Postoperative Nausea And Vomiting In Women
This study has been completed.
Sponsored by: GlaxoSmithKline
Information provided by: GlaxoSmithKline
ClinicalTrials.gov Identifier: NCT00326248
  Purpose

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.


Condition Intervention Phase
Postoperative Nausea and Vomiting
Drug: GW679769 (casopitant)
Phase III

MedlinePlus related topics: Nausea and Vomiting
Drug Information available for: Serotonin Ondansetron Ondansetron hydrochloride GW679769
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Double-Blind, Parallel Assignment, Safety/Efficacy Study
Official Title: A Phase III, Multicenter, Randomized, Double-Blind, Parallel Group Study to Evaluate the Safety and Efficacy of 50 mg 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

Further study details as provided by GlaxoSmithKline:

Primary Outcome Measures:
  • Rates of vomiting and retching [ Time Frame: after surgery ]

Secondary Outcome Measures:
  • Rates of nausea. Blood test results. [ Time Frame: after surgery ]

Enrollment: 482
Study Start Date: March 2006
Study Completion Date: July 2006
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No
Criteria

Inclusion criteria:

  • History of PONV and/or motion sickness.
  • Have not smoked for the last 6 months.
  • Having certain types of abdominal, breast or shoulder surgeries.

Exclusion criteria:

  • Pregnant or breastfeeding.
  • Taking certain medications.
  • Have certain pre-existing medical conditions.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00326248

  Show 55 Study Locations
Sponsors and Collaborators
GlaxoSmithKline
Investigators
Study Director: GSK Clinical Trials, MD, PhD GlaxoSmithKline
  More Information

Responsible Party: GSK ( Study Director )
Study ID Numbers: NKT102553
Study First Received: May 12, 2006
Last Updated: October 13, 2008
ClinicalTrials.gov Identifier: NCT00326248  
Health Authority: United States: Food and Drug Administration;   United Kingdom: Medicines and Healthcare Products Regulatory Agency;   United States: Food and Drug Administration

Keywords provided by GlaxoSmithKline:
postoperative nausea and vomiting PONV antiemetics NK-1 5HT3 casopitant mesylate ZOFRAN ondansetron hydrochloride

Study placed in the following topic categories:
Signs and Symptoms
Postoperative Nausea and Vomiting
Vomiting
Postoperative Complications
Signs and Symptoms, Digestive
Nausea
Ondansetron
Substance P
Serotonin

Additional relevant MeSH terms:
Pathologic Processes

ClinicalTrials.gov processed this record on January 14, 2009