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临床试验/NCT05130424
NCT05130424Unknown不适用

A Real-world Study of Herombopag in the Treatment of Thrombocytopenia Related Diseases in Henan Province

SuxiaLuo1 个研究点 分布在 1 个国家目标入组 498 人开始时间: 2021年9月29日最近更新:
适应症
相关药物

试验速览

阶段
不适用
发起方
入组人数
498
试验地点
1
主要终点
Incidence of adverse events after the treatment of Herombopag

研究概览

简要总结

To observe and evaluate the safety and effectiveness of herombopag in the treatment of thrombocytopenia-related diseases in Henan Province

详细描述

This study is designed as a real-world study on the treatment of thrombocytopenia-related diseases with Herombopag, to observe and analyze the safety and efficacy of Herombopag for thrombocytopenia-related diseases in the real world.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Thrombocytopenia related diseases;
  • Volunteer to join this study and sign an informed consent form;
  • Clinical evaluation can benefit from Herombopag.

排除标准

  • Those who have been confirmed to be allergic to Herombopag and/or its excipients;
  • Pregnant or breastfeeding women;
  • Except for patients with contraindications to Herombopag;
  • Doctors evaluate patients who are not suitable for inclusion.

结局指标

主要结局

Incidence of adverse events after the treatment of Herombopag

时间窗: From the treatment of Herombopag to 28 days after the end of the medication

The investigator will observe incidence of adverse events after the treatment of Herombopag, including thrombosis, diarrhea, abnormal liver function and so on.

次要结局

  • Changes of the platelet counts after the treatment of Herombopag(From the treatment of Herombopag to 28 days after the end of the medication)
  • Proportion of patients with platelet transfusion(From the treatment of Herombopag to 28 days after the end of the medication)

研究者

发起方
SuxiaLuo
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

SuxiaLuo

chief physician

Henan Cancer Hospital

研究点 (1)

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