- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04084327
Immunophenotyping of Acute b Cell Lymphoblstic Leukemia
September 9, 2019 updated by: ayat ahmed mohamed, South Egypt Cancer Institute
Immunophenotyping of Acute b Cell Lymphoblastic Leukemia
To study the immunophenotyping pattern of acute B lymphoblastic leukemia in south Egypt Cancer Institute iand its correlation with disease outcome
Study Overview
Detailed Description
study the immunophenotyping pattern of acute B lymphoblastic leukemia in south Egypt Cancer Institute from 2009 -2019 and its correlation with disease outcome
Study Type
Observational
Enrollment (Anticipated)
50
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
1 year to 80 years (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
new cases Who didn't receive treatment.Age above 1 years old.
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
overall survival outcome
Time Frame: 10 years
|
overall survival outcome
|
10 years
|
Disease-free survival outcome
Time Frame: 10 years
|
Disease-free survival outcome
|
10 years
|
association of novel CD markers with old markers for assessment of disease outcome
Time Frame: 10 years
|
association of novel CD markers with old markers for assessment of disease outcome
|
10 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
September 1, 2019
Primary Completion (Anticipated)
December 1, 2020
Study Completion (Anticipated)
December 1, 2022
Study Registration Dates
First Submitted
October 16, 2018
First Submitted That Met QC Criteria
September 9, 2019
First Posted (Actual)
September 10, 2019
Study Record Updates
Last Update Posted (Actual)
September 10, 2019
Last Update Submitted That Met QC Criteria
September 9, 2019
Last Verified
October 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- acute b All
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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