Acute Myelogenous Leukemia Clinical Trial
— HAMOfficial title:
The Clinical Observationg on HAM for Acute Myeloid Leukemia
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 |
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.
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 |
Country | Name | City | State |
---|---|---|---|
China | Shenzhen | Shenzhen | Guangdong |
Lead Sponsor | Collaborator |
---|---|
Shenzhen People's Hospital |
China,
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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