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Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of 2 doses of an approved drug for a new indication in the prevention of postoperative nausea and vomiting in patients receiving general anesthesia for open abdominal surgery requiring overnight hospital stay.


Clinical Trial Description

The duration of treatment is 4 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00090155
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Completed
Phase Phase 3
Start date September 26, 2003
Completion date November 24, 2004

See also
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