A confirmation test of the influence for hemoglobin level by consumption of the food which contain lactic acid bacteria
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000037688
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 40
Not provided
(1) Females who are received medical treatment due to anemia symptom. (2) Females who have dysmenorrhea. (3) Females who menopaused. (4) Females who have extreme unbalanced diet. (5) Subjects who having medicine, quasi-drug, Food for Specified Health Uses (FOSHU), functional indication food, supplement and/or health food within three months before starting consumption of test food. (6) Subjects who have excess meal regulation, excess diet planning and /or excess irregular meal cycle. (7) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period. (8) Subjects who have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ). (9) Subjects who excessive alcohol intake. (10) Subjects who have previous medical history of drug and/or food allergy. (11) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. (12) Subjects who are intolerant to lactose (13) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. (14) Females who donated over 400mL blood and/or blood components within the last four month to the current study. (15) Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (16) Others who have been determined ineligible by principal investigator or sub-investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method