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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04157569
Other study ID # NavyGHB-006
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date November 5, 2019
Est. completion date December 31, 2029

Study information

Verified date February 2020
Source Navy General Hospital, Beijing
Contact Liren Qian, MD
Phone +861066957676
Email qlr2007@126.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study will monitor CtDNA After Chemotherapy in Elderly Patients With AL


Description:

This study will use droplet digital PCR (ddPCR) method to quantify peripheral blood plasma mutant allele frequency (MAF) in elderly acute leukemia patients after chemotherapy to evaluate the clinical value of CtDNA .


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 31, 2029
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 60 Years to 100 Years
Eligibility Inclusion Criteria:

- Written informed consent

- Male

- not pregnant female

- patients >=60 years old

- Diagnosis of acute leukemia

Exclusion Criteria:

- Pregnancy

- HIV positive

- patients >=100 years old

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Navy General Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Navy General Hospital, Beijing

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary cumulative incidence of relapse(CIR) cumulative incidence of relapse through study completion, an average of 1 year
Secondary overall survival (OS) overall survival through study completion, an average of 2 years
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