Vitamin A Status Clinical Trial
— GloVitAS-GUOfficial title:
LOAEL/NOAEL and UL Determination in Guatemala - Estimation of Vitamin A Stores in Children and Women and Correlation With Potential Toxicity Markers
Verified date | November 2017 |
Source | Institute of Nutrition of Central America and Panama |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The goal of this study is to assess whether 3-5 years-old children who have Vitamin A intakes above the tolerable upper intake level (UL=900 ug per day) have higher total body Vitamin A stores and biomarkers of excessive vitamin A status, compared to children with Normal Vitamin A intakes (250-600 ug per day).
Status | Completed |
Enrollment | 178 |
Est. completion date | October 30, 2017 |
Est. primary completion date | September 13, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 3 Years to 5 Years |
Eligibility |
Inclusion Criteria: - Children 3-5 years old and their mothers - Child VA intake must be above 250 micrograms/day - Children must be apparently healthy, Hemoglobin>9 g/dL at recruitment point, C-reactive protein<5 mg/L. For Women, Hemoglobin>10 g/dL, C-reactive protein<5 mg/L Exclusion Criteria: °Children with Congenital or chronical diseases, reported illnesses 1 week before the test. For Women: Pregnancy or lactation, Previously known Chronic Diseases |
Country | Name | City | State |
---|---|---|---|
Guatemala | Sacatepequez City Hall | Guatemala | |
Guatemala | Mixco, La Comunidad City Hall | Guatemala City | |
Guatemala | Santa Catarina Pinula City Hall | Guatemala City |
Lead Sponsor | Collaborator |
---|---|
Institute of Nutrition of Central America and Panama | Bill and Melinda Gates Foundation, International Atomic Energy Agency, Newcastle University |
Guatemala,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Hemoglobin concentration in children | Measured with Quik Read Pro portable Device | At recruitment | |
Other | Children weight and length | Measured with Scale and Measurement Rod | At recruitment | |
Other | Systemic inflammation in children | Measured with Quik Read Pro portable Device | At recruitment | |
Other | Iron status in children | Estimated by different techniques | 28-day study period | |
Other | Zinc status in children | Estimated by atomic emission spectrometry | 28-day study period | |
Primary | Total Vitamin A stores among 3-5 years-old children, in micromoles | Estimated using Carbon 13 (13C) 13C-retinol dilution method, by the ratio of Labelled (stable isotope) versus no labelled Vitamin A in plasma 4 days after dose of labelled VA is given. | 28-day study period | |
Primary | Total dietary vitamin A intake among 3-5 years-old children, in micrograms (ug) | Estimated using 24-hour dietary recalls, observed weigh food records, food and supplement frequency questionnaire | 28-day study period | |
Secondary | Plasma retinol among 3-5 years-old children | Estimated by High Performance Liquid Chromatography (HPLC) | 28-day study period | |
Secondary | Plasma retinol binding protein among 3-5 years-old children | Estimated by ELISA | 28-day study period | |
Secondary | Plasma Transthyretin among 3-5 years-old children | Estimated by immunometric automated assay | 28-day study period | |
Secondary | Bone Health markers among 3-5 years-old children | Estimated by different techniques | 28-day study period | |
Secondary | Liver function markers among 3-5 years-old children | Estimated by different techniques | 28-day study period | |
Secondary | Plasma retinol among women | Estimated by HPLC | 28-day study period | |
Secondary | Plasma retinol binding protein among women | Estimated by ELISA | 28-day study period | |
Secondary | Plasma Transthyretin among women | Estimated by immunometric automated assay | 28-day study period | |
Secondary | Total dietary vitamin A intake among women, in micrograms (ug) | Estimated using 24-hour dietary recalls, observed weigh food records, food and supplement frequency questionnaire | 28-day study period |
Status | Clinical Trial | Phase | |
---|---|---|---|
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