Evaluating Vitamin D Content in Mushrooms
Status: | Completed |
---|---|
Conditions: | Other Indications, Gastrointestinal |
Therapuetic Areas: | Gastroenterology, Other |
Healthy: | No |
Age Range: | 18 - 64 |
Updated: | 4/21/2016 |
Start Date: | January 2012 |
End Date: | June 2013 |
Evaluation of Vitamin D in a Mushroom Supplement
This study will evaluate how much vitamin D is present in a mushroom supplement. This
supplement contains an extract from mushrooms that have been exposed to sunlight. The
mushroom supplement will be compared to non-commercially available vitamin D supplements
produced in a Goo Manufacturing Practices (GMP)-licensed facility.
supplement contains an extract from mushrooms that have been exposed to sunlight. The
mushroom supplement will be compared to non-commercially available vitamin D supplements
produced in a Goo Manufacturing Practices (GMP)-licensed facility.
Mushrooms have the capability to produce vitamin D in a similar way to human skin. When
exposed to ultraviolet light, mushrooms will convert a precursor to vitamin D. This reaction
produces large amounts of vitamin D. This study is comparing a natural source of vitamin D
to a synthetic source of vitamin D and will help determine if mushrooms are a novel source
for this essential nutrient.
exposed to ultraviolet light, mushrooms will convert a precursor to vitamin D. This reaction
produces large amounts of vitamin D. This study is comparing a natural source of vitamin D
to a synthetic source of vitamin D and will help determine if mushrooms are a novel source
for this essential nutrient.
Inclusion Criteria:
- All healthy adults, male and female, age 18-64 years
Exclusion Criteria:
- Currently taking, or having taken less than one month prior to start of study, a
prescription of 50,000 IU of vitamin D2 or 2000 IU vitamin D2 or vitamin D3
- Allergy to mushrooms
- History of elevated calcium (>10.4 mg%)
- Patients with a current or recent history of severe, progressive, and/or uncontrolled
renal, hepatic, hematological, endocrine, pulmonary, cardiac, neurological, or
cerebral disease.
- Supplementation with over the counter formulations of vitamin D2 or vitamin D3
- Subjects with a history of an adverse reaction to orally administered vitamin D.
- Subjects who are taking oral Dilantin or glucocorticoids.
- Exposure to a tanning bed or tanning on a beach for more than eight hours with no
sunscreen within 2 weeks prior to start of study.
- History of intestinal malabsorption (i.e. cystic fibrosis, fat malabsorption
syndrome, Crohn's Disease, gastric bypass surgery).
- Subjects with any other condition which in the Investigator's judgment would make the
patient unsuitable for inclusion in the study.
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