TCTR20220913005尚未招募3 期
A randomized, prospective, open-label, controlled trial comparing the efficacy of omitting H2 antagonists versus famotidine in premedication protocol for prophylaxis of taxane hypersensitivity reactions
/A0 个研究点目标入组 140 人开始时间: 2022年9月13日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 140
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
- •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)
- •3. Patients with a history of severe hypersensitivity reactions to taxanes such as bronchospasm, hypotension.
研究者
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