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NCT04024241 Clinical Trial

Medium Dose of Cytarabine and Mitoxantrone

Acute Myelogenous Leukemia Clinical Trial

— HAM  

Official title:
The Clinical Observationg on HAM for Acute Myeloid Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT04024241
Other study ID # YLi
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date September 1, 2017
Est. completion date August 31, 2019

Study information
Verified date July 2019
Source Shenzhen People's Hospital
Contact Yixuan Cao, master
Phone 15813880801
Email 358521758@qq.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 250
Est. completion date August 31, 2019
Est. primary completion date August 31, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 14 Years to 70 Years
Eligibility Inclusion Criteria:

people diagnosed as AML

Exclusion Criteria:

- acute promyeloytic leukemia

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Flow Cytometer
high dose
Drug:
• Mitoxantrone
high dose
• Cytarabine
high dose

Locations
Country Name City State
China Shenzhen Shenzhen Guangdong

Sponsors (1)
Lead Sponsor Collaborator
Shenzhen People's Hospital

Country where clinical trial is conducted

China, 

Outcome
Type Measure Description Time frame Safety issue
Primary bone marrow suppression time time of agranulocytosis one month
Primary patient survival time disease free survival three years
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