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InterNatIonal CHildhood Leukemia Microbiome/MEtabolome Cohort

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Contents

clinicaltrials.gov/study/NCT05929976
Is a
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Clinical study
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Clinical Study attributes

NCT Number
NCT059299760
Health Conditions in Trial
Microtia
Microtia
0
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Genetic predisposition
0
Acute lymphoblastic leukemia
Acute lymphoblastic leukemia
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Trial Recruitment Size
4,9000
Trial Sponsor
Columbia University
Columbia University
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Trial Collaborator
International Agency for Research on Cancer
International Agency for Research on Cancer
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Clinical Trial Start Date
October 26, 2022
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Primary Completion Date
October 1, 2029
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Study Completion Date
October 1, 2029
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Clinical Trial Study Type
Observational0
Observational Clinical Trial Type
Cohort0
Observational Study Perspective
Prospective0
Official Name
Multi-National Nutritional Biobanking Program in Pediatric Oncology InterNatIonal CHildhood Leukemia Microbiome/MEtabolome Cohort0
Last Updated
July 5, 2023
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Study summary

Nutritional status is a measurable and modifiable factor that is often not considered during treatment and its clinical impact undervalued due in part to the heavy demands on clinicians in low and middle income countries to deliver therapy to large numbers of patients. The proposed study will create a biobank of clinical data and biological specimens which will foster future studies on cancer progression and prognosis as well as toxicities during treatment which may impact survivorship and late-effects. Eligible patients must be between 3 years and 18 years of age at time of assent/consent, have newly diagnosed B- or T-cell acute lymphoblastic leukemia or mixed phenotype acute leukemia confirmed by pathology report, and must be receiving treatment at one of the participating centers. Patients receiving hematopoietic cell transplant will be excluded. Institutions were selected to ensure representation of several global health indicators related to nutritional status and wealth classification according to the World Bank. Data related to demographic variables (socioeconomic status, food security), lifestyle habits (diet, physical activity), nutritional anthropometrics (height, weight and arm anthropometry), and nutritional biological indices (stool and blood) will be collected at designated timepoints throughout treatment and one year after the end of treatment.

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