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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01296997
Other study ID # LSEP H45-10
Secondary ID
Status Completed
Phase N/A
First received February 15, 2011
Last updated November 6, 2012
Start date July 2010
Est. completion date September 2010

Study information

Verified date November 2012
Source University of Jena
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The study was conducted to investigate the effect of a calcium phosphate supplementation on the secretion of incretins.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date September 2010
Est. primary completion date September 2010
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- healthy men

Exclusion Criteria:

- intake of dietary supplements and chronic diseases

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
calcium phosphate
the subjects consumed for 3 weeks a bread enriched with 1 g pentacalcium phosphate per day
Other:
placebo
the subjects consumed a bread without pentacalcium phosphate

Locations

Country Name City State
Germany Friedrich-Schiller-University Jena, Institute of Nutrition, Department of Nutritional Physiology Jena Thuringia

Sponsors (1)

Lead Sponsor Collaborator
University of Jena

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary secretion of incretins 3 weeks Yes
Secondary concentration of minerals in plasma 3 weeks Yes
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