JPRN-UMIN000004863已完成3 期
A double-blind randomized controlled trial comparing 0.75mg of Palonosetron with 1mg of Granisetron for the control of highly emetogenic chemotherapy-induced emesis. - Trial of granisetron versus palonosetron for emesis induced by HEC(TRIPLE)
Pharma Valley Center,Shizuoka Organization for Creation Industries0 个研究点目标入组 840 人开始时间: 2011年1月12日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 840
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)known prior severe hypersensitivity to 5HT3 receptor antagonist, corticosteroids and aprepitant (2)patients who do not have enough whole body state to the antineoplastic agents treatment (3)known symptomatic brain metastasis (4)patients who has a convulsive disorders that need anticonvulsants therapy (5)patients with a symptom who has ascites or pleural effusion that need puncture (6)patients with obstruction of gastrointestinal tract,for example gastric outlet or ileus etc (7)pregnant, breastfeeding or expecting woman (8)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 (9)patients who take a medicine regularly ,for example , 5HT3 receptor antagonists, corticosteroids, antidopamine agonists, phenothiazine tranquilizers,antihistamine drugs, benzodiazepine,agents, etc (10)judged by the investigator to be inappropriate for this study
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