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NCT03286673 Clinical Trial

Comparison of Three Calcium Supplements

Healthy Clinical Trial

Official title:
Comparison of Three Calcium Supplements With Regard to Their Metabolic Effects in Healthy Adults

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03286673
Other study ID # H28-06
Secondary ID
Status Completed
Phase N/A
First received September 11, 2017
Last updated September 13, 2017
Start date October 2006
Est. completion date March 2007

Study information
Verified date September 2017
Source University of Jena
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study was conducted to investigate the metabolic effects of three different calcium compounds in healthy adults.

Recruitment information / eligibility
Status Completed
Enrollment 31
Est. completion date March 2007
Est. primary completion date March 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- age 18 - 40 years

Exclusion Criteria:

- diseases of the gastrointestinal tract

- pregnancy

- the intake of any medication (e. g. for thyroid gland)

- intake of dietary supplements

Study Design

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• calcium phosphate

• Tricalcium Phosphate

• Calcium carbonate

• Placebo

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Jena

Outcome
Type Measure Description Time frame Safety issue
Primary Serum mineral concentration Calcium and Phosphate (and others) concentration in serum. after 4 weeks of each intervention
Primary Stool mineral concentration Calcium and Phosphate concentration (and others) in stool from a three day stool collection after 4 weeks of each intervention
Primary Urine mineral concentration Calcium and Phosphate concentration (and others) in urine from a three day urine collection after 4 weeks of each intervention
Primary Lipids in blood Lipids and lipoprotein concentration in serum. after 4 weeks of each intervention
Primary Sterols Neutrals sterols and bile acids in stool from a three day stool collection after 4 weeks of each intervention
Primary Dietary intake Evaluation of the dietary intake using a three day weighed dietary record. after 4 weeks of each intervention
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