hematologic malignancies
Conditions
Interventions
course 1 aprepitant (-) course 2- aprepitant (+)
course 1 aprepitant (+) course 2- aprepitant (+)
Sponsors
Kagoshima University Hospital, division of Hematology and Immunology
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: patients (>=20 years-old) with hematologic malignancies treated with cancer chemotherapies including moderately emetogenic agents or highly emetogenic agents
Exclusion criteria
Exclusion criteria: patients unable to answer the questions about efficacy of aprepitant
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| conplete response (no vomiting, no salvage treatment) in day1 through 7. | — |
Secondary
| Measure | Time frame |
|---|---|
| complete response, frequency of nausea and vomiting, meal status, weight change | — |
Countries
Japan
Contacts
Public ContactKimiharu Uozumi
Kagoshima University Hospital Hematoilogy and Immunology
Outcome results
None listed