DRKS00009316已完成不适用
on-intervention study to the capture of the quality of life with the adult patients who receive Akynzeo to the prevention from nausea and vomiting caused by highly or moderate emetogenic chemotherapy - AkyPro NIS
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 2,173
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 Years 至 one（—）
- 性别
- All
入选标准
- •Signed patient consent form
- •Age: = 18 Years
- •1- or 2-day chemotherapy, high or moderate emetogen
- •anti-emetic prevention with Akynzeo® according to the summary of product characteristics
排除标准
- •Patients without chemotherapy
- •radiotherapy alone
- •brain tumour, symptomatic brain metastases
- •anticipatory nausea and vomiting
- •not chemotherapy-induced nausea and vomiting on the basis of other disorders or drugs
- •chemotherapies that last more than 2 days within a chemotherapy cycle
- •pregnancy
- •hypersensitivity to the active substances, excipient or other constituent materials of Akynzeo®
研究者
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