- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02720575
Evaluation of the Bioavailability of Vitamin D2 in Yeast and Bread
February 27, 2017 updated by: Michael F. Holick, Boston University
The objective of this study is to test the bioavailability of vitamin D in bread.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Vitamin D helps in reducing the risk for the development of many chronic diseases.
Humans get vitamin D mainly from direct exposure to sunlight, from diet, or from dietary supplements.
The bioavailability of vitamin D from dietary supplements has been tested.
In one study, subjects had initial vitamin D level of less than 10ng/ml, and it rose to 60ng/ml 24 hours after taking a vitamin D supplement capsule that contained 50,000 IU of vitamin D2.
Food contains vitamin D2 or vitamin D3 either naturally or after being fortified.
Fortification of dietary products date back to the first half of the 20th century when Steenbock discovered that irradiation of food helped in promoting the healing of rickets in vitamin D deficient rachitic rats.
Since that time, companies started to fortify their products to enhance their vitamin D content.
In the 1930s Bond Bread fortified its bread with vitamin D2.
Recently the FDA approved yeast vitamin D2 which is a yeast that was exposed to ultraviolet radiation.
This yeast is active and when used to raise bread the bread contains vitamin D2.
The baking process does not affect the vitamin D content.
What is unknown is whether the vitamin D2 that is produced in the bread is bioavailable.
The purpose of this study is to determine the bioavailability of vitamin D2 that is present in yeast, in bread that was raised with vitamin D2 yeast and vitamin D2 in the cell walls of yeast compared to a vitamin D2 supplement and a vitamin D3 supplement.
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 64 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy male and female adult who are free of any chronic disease
- Age 18-64 years
- BMI <30kg/m2
- No medications or disorders that would affect vitamin D metabolism
- Women must be on birth control and not pregnant based on negative pregnancy test
- Ability and willingness to give informed consent and comply with protocol
- Subjects will be included in the study regardless of their baseline vitamin D level. This is because the level is undetectable unless the subjects is taking high amount of vitamin D, and we will be excluding subjects who are taking pharmacologic doses of vitamin D of >10,000 IUs. Doses of vitamin D in supplements typically contain 400 IUs and up to 1000 IUs. Taking this amount of vitamin D will not significantly raise blood levels of vitamin D from baseline which is usually less than 5 ng/mL. Taking 1000 IUs of vitamin D will raise the blood level by approximately 1-2 ng/mL. Taking a single dose of 50,000 IUs of vitamin D raises the blood level by 50-100 ng/mL. Also a person's vitamin D status i.e. serum 25-hydroxyvitamin D does not affect how vitamin D is absorbed by the intestine nor does it influence the response of oral vitamin D on blood levels of vitamin D which is the goal of this proposal.
Exclusion Criteria:
1. Having history of hypercalcemia. 2. Taking over the counter or prescription vitamin D that is greater than 10,000 IUs daily.
3. Pregnancy. 4. History of intestinal malabsorption. 5. Inability to give informed consent. 6. Chronic hepatic or renal failure. 7. Subjects taking cholestyramine and olestra. 8. Celiac disease. 9. Allergy to wheat or gluten sensitivity.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: A
50,000 IU of crystalline D2 in 5 capsules.. Vitamin D2 in its natural state consumed orally via capsule
|
|
|
Active Comparator: B
50,000 IU of crystalline D3 in 5 capsules.. Vitamin D3 in its natural state consumed orally via capsule
|
|
|
Active Comparator: C
50,000 IU of vitamin D2 from vitamin D2 yeast in 5 capsules.
Vitamin D generated in yeast.
Acts as a comparator to the yeast in bread.
|
|
|
Active Comparator: D
50,000 IU of vitamin D2 from yeast cell walls in 5 capsules.
Yeast cell walls rich in Vitamin D. Acts as a comparator to the yeast in bread.
|
|
|
Experimental: E
50,000 IU of vitamin D2 from 2 slices of bread made from bread.
Bread raised with yeast rich in vitamin D. Main experimental arm.
|
|
|
Experimental: F
50,000 IU of vitamin D2 from 2 slices of bread.
Bread raised with yeast and yeast cell walls rich in vitamin D.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evidence of serum vitamin D levels proceeding ingestion of bread raised with yeast containing vitamin D
Time Frame: within the fist 24, 48, 72, 96, and 144 hours after ingestion
|
The subject blood will be monitored at the above mentioned time frame after consuming vitamin D in capsular or bread form.
|
within the fist 24, 48, 72, 96, and 144 hours after ingestion
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2016
Primary Completion (Actual)
December 1, 2016
Study Completion (Actual)
December 1, 2016
Study Registration Dates
First Submitted
March 22, 2016
First Submitted That Met QC Criteria
March 25, 2016
First Posted (Estimate)
March 28, 2016
Study Record Updates
Last Update Posted (Actual)
February 28, 2017
Last Update Submitted That Met QC Criteria
February 27, 2017
Last Verified
February 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-833963
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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