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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03499327
Other study ID # H5_18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 5, 2018
Est. completion date April 30, 2018

Study information

Verified date February 2023
Source University of Jena
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The interventional study will evaluate effectiveness and potential of a regularly consumption of wheat germ oil (UV treated) vs. wheat germ oil (UV untreated) to increase plasma vitamin D levels ín humans.


Description:

The interventional study in parallel design will evaluate the effectiveness and potential of a daily consumption of wheat germ oil (UV treated vs. untreated) to increase plasma vitamin D levels in humans. Wheat germ oil is naturally rich in vitamin D precursors (ergosterol and 7-dehydrocholesterol), which are converted into vitamin D2 and vitamin D3 by a defined UV light irradiation for the present study. Half of the participants will consume UV-treated wheat germ oil (intervention) and the other part will consume traditional wheat germ oil (untreated, control). The subjects will consume 10 ml of wheat germ oil per day over an entire period of 6 weeks (no follow-up). On the basis of the planned human intervention study (randomized, single-blind, parallel design) it will be investigated to what extent a regular consumption of wheat germ oil (UV-treated) can contribute to the increase of plasma 25 (OH) D levels. The comparison is made against the intake of traditional (untreated) wheat germ oil (control). The study fits with the strategy of the Competence Cluster for Nutrition and Cardiovascular Health (nutriCARD), Halle-Jena-Leipzig, Germany (www.nutriCARD.de) and the study collaborators are active members of the nutriCARD cluster.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date April 30, 2018
Est. primary completion date April 30, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria: - healthy subjects - plasma 25(OH) vitamin D < 50 nmol/l - nutritional habits: western diet Exclusion Criteria: - intake of lipid-lowering medications - gastrointestinal diseases, diabetes mellitus type I and II - intake of supplements (vitamin D supplements, fish oil capsules, vitamins and minerals) 3 months before and during the study - relevant food allergies / intolerances - visit to the solarium (within 4 weeks before beginning of the study and during the study) - stay in the mountains / skiing (within 4 weeks before beginning of studies and during the study)

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Wheat germ oil (UV treated)
Wheat germ oil is naturally rich in vitamin D precursors (ergosterol and 7-dehydrocholesterol), which are converted into vitamin D2 and vitamin D3 by a defined UV light irradiation for the present study (wheat germ oil (UV treated). The wheat germ oil (UV treated) is dispensed in dark glass bottles without label. The distinction between the groups is based on the expiration date (08.05.2018 vs. 09.05.2018). The distinction between the groups is not possible for the participants. The daily dosage of wheat germ oil is 10 ml and the study products will be consumed over an entire period of 6 weeks (no follow-up). Recommendation for intake: pure before a main meal.
Wheat germ oil (untreated)
commercial available wheat germ oil The wheat germ oil (untreated) is dispensed in dark glass bottles without label. The distinction between the groups is based on the expiration date (08.05.2018 vs. 09.05.2018). The distinction between the groups is not possible for the participants. The daily dosage of wheat germ oil is 10 ml and the study products will be consumed over an entire period of 6 weeks (no follow-up). Recommendation for intake: pure before a main meal.

Locations

Country Name City State
Germany Friedrich-Schiller-University Jena Thuringia

Sponsors (2)

Lead Sponsor Collaborator
University of Jena Martin-Luther-Universität Halle-Wittenberg

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vitamin D status plasma levels of 25OHD2, 25OHD3 (nmol/l) change from baseline after 3 and 6 weeks
Secondary Blood lipids total cholesterol, LDL cholesterol, HDL cholesterol, triacylglycerides (mmol/L) change from baseline after 3 and 6 weeks
Secondary Blood glucose fasting blood glucose (mmol/l) change from baseline after 3 and 6 weeks
Secondary Insulin insulin (units/ml) change from baseline after 3 and 6 weeks
Secondary soluble Klotho (sKlotho) sKlotho is a component of the FGF23 system and is associated with longevity change from baseline after 3 and 6 weeks
Secondary Fibroblast growth factor 23 (FGF23) FGF23 is a regulator of vitamin D metabolism and also a risk factor for heart failure change from baseline after 3 and 6 weeks
Secondary Fatty acid distribution (erythrocytes) fatty acid distribution in erythrocyte lipids (% fatty acid methyl ester) change from baseline after 3 and 6 weeks
Secondary Vitamin D forms 1 1,25(OH)2D2 (nmol/l) change from baseline after 3 and 6 weeks
Secondary Vitamin D forms 2 1,25(OH)2D3 (nmol/l) change from baseline after 3 and 6 weeks
Secondary Vitamin D forms 3 24,25(OH)2D (nmol/l) change from baseline after 3 and 6 weeks
Secondary Vitamin D forms 4 20(OH)D (nmol/l) change from baseline after 3 and 6 weeks
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