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Status unknownNCT04024241HAMUpdated Jul 18, 2019

Medium Dose of Cytarabine and Mitoxantrone

An observational study in Acute Myelogenous Leukemia and Chemotherapy, sponsored by Shenzhen People's Hospital. Status unknown at 1 site in China. Open to participants aged 14 Years to 70 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-07-18.

Sponsored by Shenzhen People's Hospital · Observational

The sponsor has not verified this record recently (last verified Jul 2019), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
250
Ages
14 Years to 70 Years
Sex
All
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Study 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.

Read the detailed 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.

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Conditions studied

  • Acute Myelogenous Leukemia
  • Chemotherapy

Keywords

  • AML HAM
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In context

Leukemia

5,441 studies on the registry are indexed under Leukemia; 637 are open to participants now.

This study's planned enrollment of 250 is above the median of 120 across 744 observational studies indexed under Leukemia.

Browse Leukemia studies →

Lead sponsor

Shenzhen People's Hospital is the lead sponsor of 62 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

people diagnosed as AML expect acute promyeloytic leukemia

Inclusion criteria

people diagnosed as AML

Exclusion criteria

Exclusion Criteria:

  • acute promyeloytic leukemia
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Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
250 participants (estimated)
Patient registry
No

Groups and cohorts

  • high dose of cytarabine

    high dose of cytarabine

    Device: Flow Cytometer · Drug: Mitoxantrone · Drug: Cytarabine

  • HAM

    medium dose of cytarabine and mitoxantrone

    Device: Flow Cytometer · Drug: Mitoxantrone · Drug: Cytarabine

Interventions

  • DeviceFlow Cytometer

    high dose

  • DrugMitoxantrone

    high dose

  • DrugCytarabine

    high dose

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What researchers measure

Primary outcomes

  1. bone marrow suppression time

    time of agranulocytosis

    Time frame: one month

  2. patient survival time

    disease free survival

    Time frame: three years

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Study locations

1 of 1 sites recruiting
  • Shenzhen
    Shenzhen, Guangdong 518000, China
    Recruiting
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 18, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04024241
Lead sponsor
Shenzhen People's Hospital
Responsible party
Sponsor
First posted
Jul 18, 2019
Start date
Sep 1, 2017
Primary completion
Aug 31, 2019 (estimated)
Completion
Aug 31, 2019 (estimated)
Last update
Jul 18, 2019

Study contacts

Yixuan Cao, master
Contact
358521758@qq.com
15813880801

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2019. You cannot join it, but the record below documents what was studied.

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