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临床试验/NCT04024241
NCT04024241Unknown不适用

The Clinical Observationg on HAM for Acute Myeloid Leukemia

Shenzhen People's Hospital1 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2017年9月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
入组人数
250
试验地点
1
主要终点
patient survival time

研究概览

简要总结

By observation of the inpatients in shenzhen people's hospital,research the curative effect of the two chemotherapy schemes on AML-High dose of cytarabine and HAM.

详细描述

The patients of AML in shenzhen people's hospital were randomly divided into two therapy groups.One group was treated by High dose of cytarabine ,and the other was HAM.Evaluate the two chemotherapy schemes by bone marrow suppression time and patient survival time.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Cross Sectional

入排标准

年龄范围
14 Years 至 70 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • people diagnosed as AML

排除标准

  • acute promyeloytic leukemia

研究组 & 干预措施

high dose of cytarabine

high dose of cytarabine

干预措施: Flow Cytometer (Device)

high dose of cytarabine

high dose of cytarabine

干预措施: Mitoxantrone (Drug)

high dose of cytarabine

high dose of cytarabine

干预措施: Cytarabine (Drug)

HAM

medium dose of cytarabine and mitoxantrone

干预措施: Flow Cytometer (Device)

HAM

medium dose of cytarabine and mitoxantrone

干预措施: Mitoxantrone (Drug)

HAM

medium dose of cytarabine and mitoxantrone

干预措施: Cytarabine (Drug)

结局指标

主要结局

patient survival time

时间窗: three years

disease free survival

bone marrow suppression time

时间窗: one month

time of agranulocytosis

次要结局

未报告次要终点

研究者

发起方
Shenzhen People's Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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