Vitamin A Status Clinical Trial
Verified date | March 2008 |
Source | Tufts University |
Contact | n/a |
Is FDA regulated | No |
Health authority | Zimbabwe: Medical Research Council |
Study type | Interventional |
The study hypothesis is that high ß-C yellow maize can provide vitamin A efficiently.
- list item one ß-C in yellow maize
The study will use stable isotope labeled high ß-C yellow maize and vitamin A in a
well-nourished population by utilizing stable isotope dilution techniques. In this project,
deuterium labeled vitamin A that is derived from the labeled ß-C yellow maize will be traced
after being eaten by a human subject. Eight men (> 40 years and < 70 y) who are healthy,
non-smoking,body weight within 20% of standard weight for height (Metropolitan) and not
having taken vitamin A or ß-C supplements within the last month will be recruited as
volunteers. This study will last for 50 days during which at day 1, cooked labeled yellow
maize paste (porridge) equal to a total of ~ 2 bowls cooked yellow maize (from 100 - 200 g
dry weight) containing ~ 1 mg ß-C will be taken by each volunteer. On day 8, a labeled
vitamin A (1 mg of 13C retinyl acetate) in oil dose will be used in evaluation of liver
storage of vitamin A. Forty six blood samples (460 cc) will be taken during the study which
will be analyzed for serum carotenoids and retinoids using HPLC and mass spectrometry
techniques.
The serum concentration and isotope ratio of ß-C and retinol will be determined. Serum
enrichment curve following each oral dose will be studied. The area under the curve (AUC) of
retinol-d4 and labeled retinol from the reference dose in serum samples will be determined
and compared. The equivalence of a high ß-C corn meal to vitamin A will be calculated based
on the isotope reference method to determine the efficiency of corn ß-C to provide vitamin
A.
Status | Completed |
Enrollment | 8 |
Est. completion date | March 2008 |
Est. primary completion date | March 2008 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 40 Years to 70 Years |
Eligibility |
Inclusion Criteria: - healthy subjects Exclusion Criteria: - GI track problems |
Allocation: Non-Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science
Country | Name | City | State |
---|---|---|---|
Zimbabwe | National University of Science and Technology | Bulawayo |
Lead Sponsor | Collaborator |
---|---|
Tufts University | National University of Science and Technology, Zimbabwe, Nutricia Research Fundation |
Zimbabwe,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Bioavailability of corn beta-carotene and its equivalency to provide vitamin A | one year | No |
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