Patients receiving highly or moderately emetogenic agents
Conditions
Interventions
None listed
Sponsors
Kobe City Medical Center General Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1)Adult 2)Patients receiving highly or moderately emetogenic agents 3)A consent form for participating in this study is submitted
Exclusion criteria
Exclusion criteria: 1)Patients having past history of hypersensitivity to fosaprepitant 2)Used Pimozide
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1)CTCAE ver.4.0 2)MAT | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)Questionnaire of convenience 2)Toxicity and side effect | — |
Countries
Japan
Contacts
Public ContactAkihito Tsuji
Kobe City Medical Center General Hospital Department of Medical oncology
Outcome results
None listed