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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 12 December 2020
Main ID:  NCT03471416
Date of registration: 14/03/2018
Prospective Registration: Yes
Primary sponsor: Columbia University
Public title: Nutritional Status in Children With ALL in Guatemala
Scientific title: Nutritional Status in Children With Acute Lymphoblastic Leukemia Undergoing Treatment at the National Pediatric Oncology Unit in Guatemala City, Guatemala
Date of first enrolment: May 1, 2019
Target sample size: 60
Recruitment status: Recruiting
URL:  https://clinicaltrials.gov/show/NCT03471416
Study type:  Observational
Study design:   
Phase: 
Countries of recruitment
Guatemala
Contacts
Name:     Elena J Ladas, RD, PhD
Address: 
Telephone: 212.305.7835
Email: ejd14@cumc.columbia.edu
Affiliation: 
Name:     Federico Antiloon, MD, MMM, PhD
Address: 
Telephone:
Email:
Affiliation:  Unidad Nacional de Oncología Pediátrica
Name:     Elena J Ladas, RD, PhD
Address: 
Telephone:
Email:
Affiliation:  Columbia University
Name:     Federico Antiloon, MD, MMM, PhD
Address: 
Telephone:
Email: fantillo@ufm.edu
Affiliation: 
Name:     Ronald Barr, MB, ChB, MD
Address: 
Telephone:
Email:
Affiliation:  McMaster University
Key inclusion & exclusion criteria

Inclusion Criteria:

- Children under treatment for Acute Lymphoblastic Leukemia (ALL)

- Age under 18 years

- Getting treatment at UNOP

Exclusion Criteria:

- If they can't participate in the study due to illness or long distance to travel to
UNOP



Age minimum: 3 Years
Age maximum: 18 Years
Gender: All
Health Condition(s) or Problem(s) studied
Acute Lymphoblastic Leukemia
Intervention(s)
Primary Outcome(s)
Association of BMI and Body Composition [Time Frame: Up to 6 months after treatment]
Association of MUAC and Body Composition [Time Frame: Up to 6 months after treatment]
Association of TSFT and Body Composition [Time Frame: Up to 6 months after treatment]
Secondary Outcome(s)
Habitual Activity Estimation Scale [Time Frame: Up to 6 months after treatment]
Body Composition [Time Frame: Up to 6 months after treatment]
Secondary ID(s)
AAAR4744
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Unidad nacional de Oncologia Pediatrica, Guatemala
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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