Metabolic Syndrome Clinical Trial
Official title:
Bioavailability and Biological Effects of Vitamin D2 Contained in Mushroom
Verified date | April 2017 |
Source | Icahn School of Medicine at Mount Sinai |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to compare the safety and efficacy of two different amounts of
vitamin D2 (600 or 4000 International Units/day) provided by mushrooms added to one of the
daily meals versus same doses of vitamin D3 provided as oral supplements sold in any
drugstore in reaching adequate or optimal blood levels of 25(OH)D in people with Vitamin D
deficiency and pre-diabetes (high blood sugar without full blown diabetes) or the metabolic
syndrome. Metabolic syndrome is the name of a group of risk factors that raise the risk for
heart disease and other health problems, such as diabetes and stroke as described by the US
department of Health and Human Services.
This study will also attempt to demonstrate and compare the effect of the intervention with
above two doses of vitamin D on blood levels of tests that show inflammation.
Status | Completed |
Enrollment | 47 |
Est. completion date | September 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years to 90 Years |
Eligibility |
Inclusion Criteria: - Adult non-smoking subjects from ages 30 to 90, any race or gender - Presence of at least two of the following characteristics: - Waist circumference: Men: > 102 cm Women: > 88 cm - Blood pressure: > 130/85 mm Hg (or use of anti-BP medication) - HDL-cholesterol: Men: < 40 mg/dL Women: < 50 mg/dL - Triglycerides: > 150 mg/dL (or use of medications for high triglycerides such as fibrates or nicotinic acid) - Fasting blood sugar > 100 mg/dl (or use of metformin), but a HbA1c < 6.5% Exclusion Criteria: - Blood levels of 25(OH)D > 50 nmol/L - Regular intake of vitamin D fortified milk exceeding approximately 3 glasses/day - Lack of the ability to comprehend instructions and/or sign the consent form - Inability to comply with the potential requirement to eat a daily portion of provided mushroom together with meals - Inability to comply with the rule of avoiding any beach days during the duration of the study - Any projected trip to sunny places such as Puerto Rico and the Caribbean during the period of study - Any attendance to tanning studios during the period of study - Women who regularly use a veil over their heads - Any history of kidney stone formation - Non-traumatic bone fracture over the past 3 years - Any form of vitamin D supplement intake, including combined calcium and vitamin D products - Active smoking |
Country | Name | City | State |
---|---|---|---|
United States | Icahn School of Medicine at Mount Sinai | New York | New York |
Lead Sponsor | Collaborator |
---|---|
Icahn School of Medicine at Mount Sinai |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 25OH Vitamin D level | To compare the efficacy of two different doses of vitamin D2 (600 or 4000 IU/day) provided by Vitamin D2 fortified mushrooms added to one of the daily meals versus same doses of vitamin D3 provided as oral supplements in reaching adequate or optimal circulating levels of 25(OH) D in a racially diverse group of subjects with Vitamin D deficiency and pre-diabetes or the metabolic syndrome. | at 4 months | |
Secondary | Serum calcium | To assess the safety of the intervention with respect to serum calcium levels in all study subjects. Measured at each study visit (1, 2, 3, and 4 months) | at 1 month | |
Secondary | Serum calcium | To assess the safety of the intervention with respect to serum calcium levels in all study subjects. Measured at each study visit (1, 2, 3, and 4 months) | at 2 months | |
Secondary | Serum calcium | To assess the safety of the intervention with respect to serum calcium levels in all study subjects. Measured at each study visit (1, 2, 3, and 4 months) | at 3 months | |
Secondary | Serum calcium | To assess the safety of the intervention with respect to serum calcium levels in all study subjects. Measured at each study visit (1, 2, 3, and 4 months) | at 4 months | |
Secondary | Markers of inflammation and metabolic control | To demonstrate and compare the effect of the intervention with above two doses of vitamin D on circulating levels of markers of inflammation and metabolic control (CRP, tumor necrosis factor (TNF), hemoglobin A1c, insulin, blood glucose, lipids). | at 4 months |
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