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临床试验/JPRN-UMIN000009702
JPRN-UMIN000009702已完成2 期

Efficacy of Aprepitant for Hematology and Oncology. - Efficacy of Aprepitant for Hematology and Oncology.

Kyoto University Hospital,Department of Hematology and Oncology0 个研究点目标入组 30 人开始时间: 2013年1月20日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
30

研究概览

简要总结

Frequency of nausea and vomitting decreased with the addition of aprepitant.

研究设计

研究类型
Interventional

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. chemotherapy within 6 days before study day 1 or between days 1 to 6. 2.Antiemetic therapy prior to 48 hr of chemotherapy. 3.Corticosteroids therapy within 72 hr before study day 1 or duration of study 4.Radiation therapy to the abdomen or pelvis within 6 days before study day 1 or duration of study 5.known central nervous system malignancy 6.following drug therapy within 6 days before study day 1 - clarithromycin, ketoconazole, itraconazole - 7. following drug therapy within 4 weeks before study day 1 - barbiturate, rifampicin, phenytoin, carbamazepine - 8. pregnant, nursing or possibly pregnant women 9.Patients judged inappropriate for this study by physicians

研究者

发起方
Kyoto University Hospital,Department of Hematology and Oncology

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