323
Participants
Start Date
September 30, 2011
Primary Completion Date
August 31, 2017
Study Completion Date
December 31, 2017
Dexamethasone, Ondansetron, Aprepitant
Arm B participants will be given doses of anti-emetics based on the emesis risk calculation. Doses will vary depending on the which level they fall into level 0, level 1, 2 or 3 based on the participant's diary.
Arm A: Standard Anti-emetic regimen
Treating physician's discretion for type of anti-emetic to be prescribed.
The Ottawa Hospital Cancer Centre, Ottawa
Lead Sponsor
Ottawa Hospital Research Institute
OTHER