IRCT2015040121574N1已完成早期 1 期
Effect of increase in duration of Aprepitant consumption from 3 to 6 days on the prevention of nausea and vomiting in women receiving combination of Anthracycline/Cyclophosphamide chemotherapy: A randomized, crossover, clinical trial
Vice chancellor for research, Esfahan university of medical science0 个研究点目标入组 49 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 49
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
- 24 years 至 50 years（—）
- 性别
- Female
入选标准
- •General inclusion criteria: Less than 50 years of age, diagnosed with breast cancer and scheduled to receive 4 courses Anthracycline/Cyclophosphamide (AC) regimens.
- •General exclusion criteria: previous history of gastritis, diabetes and brain tumor.
排除标准
- 未提供
研究者
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