Topic: Generic Health Relevance and Cross Cutting Themes
Conditions
Interventions
The intervention will last 14 days. However, first contact with the study participants will be 2 months prior to the start of the intervention to explain the study. A capsule containing 2 mg dose of b
Sponsors
Newcastle University (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Aged 18 - 45 years 2. Generally fit and healthy adults 3. Males and females
Exclusion criteria
Exclusion criteria: 1. Smokers 2. Pregnant females 3. Diabetics 4. Liver disease 5. Gastrointestinal disorders
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood concentrations of administered beta-carotene/retinyl acetate, and derived metabolites. Primary outcome measures will be taken at 0, 2, 4, 6, 8, 12 hours on day 1. Then at days 2, 3, 7, and 14. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcome measures | — |
Countries
United Kingdom
Outcome results
None listed