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NCT00334152 · ClinicalTrials.gov registry record · Phase 3
Casopitant And ZOFRAN To Prevent Post Operative Nausea And Vomiting In Women
A Phase 3 study of Postoperative Nausea and Vomiting and Nausea and Vomiting, Postoperative, sponsored by GlaxoSmithKline.
- Completed
- Registry status
- Phase 3
- Development phase
- 515
- Enrollment target
- 20
- Study locations
NCT00334152 is a Phase 3 study of Postoperative Nausea and Vomiting and Nausea and Vomiting, Postoperative that has completed, run by GlaxoSmithKline. The registered enrollment target is 515 participants, above the 414-participant average among 9 other Postoperative Nausea and Vomiting trials with a reported enrollment target (24% higher). The trial reports 20 study locations across 10 states.
The verdict
NCT00334152, a Phase 3 study of Postoperative Nausea and Vomiting and Nausea and Vomiting, Postoperative, has completed, sponsored by GlaxoSmithKline.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 515 participants
- Enrollment target
- 20
- Study locations
Study Summary
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.
Conditions Studied
Interventions
- DRUG casopitant
Study Locations (20)
California
- GSK Investigational Site - Arcadia
- GSK Investigational Site - Glendale
- GSK Investigational Site - Laguna Hills
- GSK Investigational Site - Pasadena
Florida
- GSK Investigational Site - Boca Raton
- GSK Investigational Site - Melbourne
- GSK Investigational Site - Miami
- GSK Investigational Site - West Palm Beach
Alabama
- GSK Investigational Site - Fairhope
- GSK Investigational Site - Mobile
- GSK Investigational Site - Montgomery
New York
- GSK Investigational Site - Mineola
- GSK Investigational Site - New Hyde Park
- GSK Investigational Site - New York
Arkansas
- GSK Investigational Site - Little Rock
Illinois
- GSK Investigational Site - Chicago
Kansas
- GSK Investigational Site - Kansas City
Maryland
- GSK Investigational Site - Baltimore
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 515 participants |
| Start Date | 2006-03 |
| Est. Completion | 2006-07 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00334152
The ClinicalTrials.gov registry entry for NCT00334152 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 515 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 414-participant average among 9 other Postoperative Nausea and Vomiting trials with a reported enrollment target (24% higher). The listed sponsor is GlaxoSmithKline, which has 1,345 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Postoperative Nausea and Vomiting appearing as the primary indexed condition, and to 1 intervention - of which casopitant is the first listed.
NCT00334152 reports 20 study locations spanning 10 distinct geographic areas - top geographies include California, Florida, Alabama.
Frequently Asked Questions
What is clinical trial NCT00334152 about?
NCT00334152 is a clinical study titled "Casopitant And ZOFRAN To Prevent Post Operative Nausea And Vomiting In Women". 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.
What is the current status of trial NCT00334152?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 515 participants. The study started on 2006-03. Estimated completion is 2006-07.
What conditions does trial NCT00334152 study?
This clinical trial studies the following conditions: Postoperative Nausea and Vomiting, Nausea and Vomiting, Postoperative.
What interventions are being tested in trial NCT00334152?
The interventions under investigation include: casopitant (DRUG).
Who is sponsoring clinical trial NCT00334152?
This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00334152 being conducted?
This trial has 20 study locations across Alabama, Arkansas, California, Florida, Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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