ITMCTR2100004548招募中4 期
Post marketing safety evaluation of Fufang Congrong Yizhi Capsule
适应症
试验速览
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational study
入排标准
- 年龄范围
- 50 至 80（—）
- 性别
- All
入选标准
- •(1) All the inpatients and / or outpatients who used compound Cistanche yizhi capsule at least once, regardless of the duration of medication, were regarded as the monitoring population;
- •(2) Outpatients and inpatients with vascular dementia (may have comorbidities);
- •(3) The patient or his / her legal representative informed the research purpose, method and possible risks in a clear and normal mental state, did not interfere with the decision of the patient or his / her legal agent, agreed to participate in the study, and signed the informed consent.
排除标准
- •(1) Loose stool;
- •(2) Patients with serious diseases such as heart, brain, liver, kidney or hematopoietic system;
- •(3) Abnormal liver and kidney function, abnormal ECG with clinical significance;
- •(4) Known to be allergic to the components of compound Congrong yizhi capsule;
- •(5) Patients are participating in other clinical trials.
研究者
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