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临床试验/JPRN-UMIN000017486
JPRN-UMIN000017486已完成未知

A phase II study of aprepitant, palonosetron, dexamethasone and olanzapine for the prevention of cisplatin-based hemotherapy-induced nausea and vomiting for thoracic malignancy - A phase II study of aprepitant, palonosetron, dexamethasone and olanzapine for the prevention of cisplatin-based hemotherapy-induced nausea and vomiting for thoracic malignancy

Shizuoka cancer center0 个研究点目标入组 30 人开始时间: 2015年5月10日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1) Prior severe hypersensitivity to aprepitant, 5HT3 receptor antagonist, corticosteroids or olanzapine 2) Patients who do not have enough whole body state to the antineoplastic agents treatment 3) Severe complication 4) Patients who have conceived child or desire childbearing or breast-feed their baby 5) Patients enforced radiotherapy at the bottom of diaphragm on the period between 6 days before and 6 days after of the date of first therapy 6) Patients who cannot stay in hospital till the 6th day of chemotherapy 7) HbA1c (NGSP) >= 6.5. FBS >= 126mg/dl or BS >= 200mg/dl 8) Diabetes mellitus 9) Patient with nausea and vomiting needing for medical treatment beore chemotherapy 10) Patient who have previous history or familial history of malignant syndrome 11) CK more than 2.5 times of institutional upper normal limit 12) Patients with active infection 13) Patient who cannot stop smoking during this study 14) BMI (body mass index) >= 35 15) Patients who take a medicine regularly ,for example , 5HT3 receptor antagonists, corticosteroids, antidopamine agonists, phenothiazine tranquilizers,antihistamine drugs, benzodiazepine,agents, etc

研究者

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