22
Participants
Start Date
August 31, 2006
Primary Completion Date
December 31, 2009
Study Completion Date
August 31, 2012
aprepitant
Given PO
gemcitabine hydrochloride
Given IV
capecitabine
Given PO
fluorouracil
Given IV
radiation therapy
Undergo radiation therapy
questionnaire administration
Ancillary studies
quality-of-life assessment
Ancillary studies
nausea and vomiting therapy
Receive aprepitant
management of therapy complications
Receive aprepitant
Wake Forest University Health Sciences, Winston-Salem
National Cancer Institute (NCI)
NIH
Merck Sharp & Dohme LLC
INDUSTRY
Wake Forest University Health Sciences
OTHER