None listed
Conditions
Interventions
Intervention1: Stable isotope labelled cyanocobalamin: Stable Isotopically labelled 13C cyanocobalamin (2.0 ug) dose will be orally administered on the study day. Stable isotopically labelled 13C cyan
Sponsors
DBTWellcome Trust India Alliance
Eligibility
Inclusion criteria
Inclusion criteria: Healthy adult individuals with normal clinical history, good general health and with normal blood biochemistry will be recruited.
Exclusion criteria
Exclusion criteria: Exclusion criteria are allergies, intolerances, hypersensitivity, severe anemia, medication use, history of infectious diseases, physical or psychiatric or surgical intervention.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Vitamin B12 status and its bioavailabilityTimepoint: One time measurement with biospecimen collection over 12 hrs after the dose administration | — |
Secondary
| Measure | Time frame |
|---|---|
| Genetic variants and their role in understanding the B12 deficiency and colonic absorption of vitamin B12Timepoint: Baseline for genetic variants and One time measurement with biospecimen collection over 4 hrs after the dose administration for colonic absorption | — |
Countries
India
Contacts
Public ContactDr Sarita Devi
St. Johns Research Institute
Outcome results
None listed