JPRN-UMIN000003979招募中未知
A pilot study of efficacy and safety of aprepitant with chemoradiotherapy involving weekly cisplatin in patients with cervical cancer. - A pilot study of aprepitant with CCRT
ara Medical University0 个研究点目标入组 30 人开始时间: 2010年8月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 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
- Female
入选标准
- 未提供
排除标准
- •1. patients with received pimozide. 2. patients with history of chemotherapy with cisplatin. 3. patients with vomiting within 24 hours before first administrating of cisplatin. 4. patients who have had any other cancer. 5. patients who are pregnant or breast feeding. 6. patients with severe complications (heart disease, uncontrolled diabetes,bleeding tendency). 7. patients with active infection disease whom steroid is inappropriate for. 8. patients who have a history of hypersensitivity to drugs. 9. patients who were administered drugs in the following, 5-HT3 blocker, phenothiazine, butyrophenone, benzamide, dopamine receptor antagonist. 10. patients who are considered to be inappropriate for this study judged by the treating physician.
研究者
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