TCTR20210322004已完成3 期
Efficacy of Premedication Protocol Without Ranitidine for Taxane Regimen : A Multicenter Non-Randomized Historical Controlled Study
/A0 个研究点目标入组 221 人开始时间: 2021年3月22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
- 221
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
- 18 Years 至 80 Years（—）
- 性别
- All
入选标准
- •1. Cancer patients who received taxane chemotherapy regimen
排除标准
- •1.History of severe Hypersensitivity reactions from taxane regimen
- •2.Severe hepatic impairment (bilirubin >5xULN or AST/ALT >10xULN)
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