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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04084327
Other study ID # acute b All
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date September 1, 2019
Est. completion date December 1, 2022

Study information

Verified date October 2018
Source South Egypt Cancer Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To study the immunophenotyping pattern of acute B lymphoblastic leukemia in south Egypt Cancer Institute iand its correlation with disease outcome


Description:

study the immunophenotyping pattern of acute B lymphoblastic leukemia in south Egypt Cancer Institute from 2009 -2019 and its correlation with disease outcome


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 50
Est. completion date December 1, 2022
Est. primary completion date December 1, 2020
Accepts healthy volunteers No
Gender All
Age group 12 Months to 80 Years
Eligibility Inclusion Criteria:

- New cases admitted to SECI Who didn`t receive treatment.Age above 1 years old.

Exclusion Criteria:

- Cases who received treatment Patients below 1 years old.Patients diagnosed as AML or T-ALL

Study Design


Related Conditions & MeSH terms


Intervention

Other:
stastical analysis
1-Clinical examination data-Complete Blood Count (CBC).Bone Marrow Aspiration (BMA)-Bone Marrow Biopsy (BMB). (if available)-Immunophenotyping results (IPT).Cytogenetic results

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
South Egypt Cancer Institute

References & Publications (1)

Keegan A, Charest K, Schmidt R, Briggs D, Deangelo DJ, Li B, Morgan EA, Pozdnyakova O. Flow cytometric minimal residual disease assessment of peripheral blood in acute lymphoblastic leukaemia patients has potential for early detection of relapsed extramedullary disease. J Clin Pathol. 2018 Jul;71(7):653-658. doi: 10.1136/jclinpath-2017-204828. Epub 2018 Mar 27. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary overall survival outcome overall survival outcome 10 years
Primary Disease-free survival outcome Disease-free survival outcome 10 years
Primary association of novel CD markers with old markers for assessment of disease outcome association of novel CD markers with old markers for assessment of disease outcome 10 years
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