Calcium Phosphate and Incretins
This study has been completed.
Sponsor:
University of Jena
Information provided by (Responsible Party):
Gerhard Jahreis, University of Jena
ClinicalTrials.gov Identifier:
NCT01296997
First received: February 15, 2011
Last updated: November 6, 2012
Last verified: November 2012
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Purpose
The study was conducted to investigate the effect of a calcium phosphate supplementation on the secretion of incretins.
| Condition | Intervention |
|---|---|
|
Healthy Men |
Dietary Supplement: calcium phosphate Other: placebo |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Influence of a Calcium Phosphate Supplementation on the Secretion of Incretins in Humans. |
Resource links provided by NLM:
MedlinePlus related topics:
Calcium
Drug Information available for:
Calcium Gluconate
U.S. FDA Resources
Further study details as provided by University of Jena:
Primary Outcome Measures:
- secretion of incretins [ Time Frame: 3 weeks ] [ Designated as safety issue: Yes ]
Secondary Outcome Measures:
- concentration of minerals in plasma [ Time Frame: 3 weeks ] [ Designated as safety issue: Yes ]
| Enrollment: | 10 |
| Study Start Date: | July 2010 |
| Study Completion Date: | September 2010 |
| Primary Completion Date: | September 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: calcium phosphate |
Dietary Supplement: calcium phosphate
the subjects consumed for 3 weeks a bread enriched with 1 g pentacalcium phosphate per day
|
| Placebo Comparator: placebo |
Other: placebo
the subjects consumed a bread without pentacalcium phosphate
|
Eligibility| Ages Eligible for Study: | 20 Years to 35 Years |
| Genders Eligible for Study: | Male |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- healthy men
Exclusion Criteria:
- intake of dietary supplements and chronic diseases
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01296997
Locations
| Germany | |
| Friedrich-Schiller-University Jena, Institute of Nutrition, Department of Nutritional Physiology | |
| Jena, Thuringia, Germany, 07743 | |
Sponsors and Collaborators
University of Jena
Investigators
| Principal Investigator: | Gerhard Jahreis, Prof. Dr. | Friedrich-Schiller-University Jena, Institute of Nutrition, Department of Nutritional Physiology |
More Information
No publications provided by University of Jena
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Gerhard Jahreis, Prof. Dr. habil, University of Jena |
| ClinicalTrials.gov Identifier: | NCT01296997 History of Changes |
| Other Study ID Numbers: | LSEP H45-10 |
| Study First Received: | February 15, 2011 |
| Last Updated: | November 6, 2012 |
| Health Authority: | Germany: Ethics Commission |
Keywords provided by University of Jena:
|
calcium phosphate incretins human study |
Additional relevant MeSH terms:
|
Calcium, Dietary Incretins Bone Density Conservation Agents Physiological Effects of Drugs |
Pharmacologic Actions Hormones Hormones, Hormone Substitutes, and Hormone Antagonists |
ClinicalTrials.gov processed this record on June 17, 2013