A Double-Blind, Cross-over Study on Effect of the Single Ingestion of Milk Proteins and Milk Oligosaccharide on Mineral Absorption.
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000053417
- Lead Sponsor
- Hokkaido Information University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 30
Not provided
1.Subjects who are under physician's advice, treatment, and/or medication for diabetes, renal disease, galactosemia, osteoporosis, thyroid dysfunction, hypertension, dyslipidemia, gastrointestinal diseases. 2.Subjects who use pacemakers and/or defibrillators. 3.Subjects with serious cerebrovascular, cardiac, hepatic, renal, gastrointestinal, respiratory diseases, and/or affected with infectious diseases requiring reports to the authorities. 4.Subjects with major surgical history relevant to the digestive system. 5.Subjects with unusually high and/or low blood pressure, abnormal physical data and/or abnormal hematological data. 6.Subjects with severe anemia. 7.Post-menopausal women complaining of obvious physical changes. 8.Subjects who are at risk of having allergic reactions to drugs and/or foods especially based on milk, eggs, wheat, sesame, mackerel, soy beans, apples, etc. 9.Subjects with lactose intolerance, and/or who be unable to drink a cup of milk (200 ml) within 5 minutes. 10.Subjects who regularly take medicine, functional foods, and/or supplements which would affect mineral absorption. 11.Heavy smokers, alcohol addicts or subjects with disordered lifestyle. 12.Subjects who donated either 400 ml whole blood within 16 wks, 200 ml whole blood within 4 wks, or blood components within 2 wks, prior to this study. 13.Pregnant or lactating women or women who expect to be pregnant. 14.Subjects who currently participate in other clinical trials, or participated within the last 4 wks prior to this study. 15.Subjects who are ineligible due to physician's judgment.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method