Developing Individualized Strategies to Prevent Nausea and Vomiting
Interventional
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Incidence of post-discharge nausea and vomiting (PDNV)
48 hours post-discharge
No
United States: Institutional Review Board
1R01CA163074-01A1
NCT01393288
April 2012
November 2015
Name | Location |
---|---|
University of Kansas Medical Center | Kansas City, Kansas 66160-7353 |
University of California, San Francisco | San Francisco, California 94143 |
Cleveland Clinic | Cleveland, Ohio 44195 |
Ohio State University Medical Center | Columbus, Ohio 43210 |
Brigham & Women's Hospital | Boston, Massachusetts 02115 |
University of Kentucky Hospital | Lexington, Kentucky 40536 |