A study of improvement effects on salivary secretion by ingesting a food ingredient.
- Conditions
- Healthy female adults
- Registration Number
- JPRN-UMIN000047976
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 60
Not provided
(1) Subjects who routinely use the health-specific/functional/supplementary/health foods which may affect this study (more than three times a week), and have any difficulty in stopping use after the consent. (2) Subjects who have used medicines which may affect this study, more than two days a week, and have any difficulty in limiting use during this study. (3) Subjects who are planning to visit the hospital for cavity protection or oral cleaning during this study. (4) Subjects who have been determined as dry mouth symptom and/or Sjogren's syndrome. (5) Subjects with smoking habit, now and/or within a year before this study. (6) Subjects who drink a lot of alcohol. (7) Subjects having some kind of serious/progressive disease and symptom. (8) Subjects with previous/present medical history of serious diseases in heart, liver, kidney and digestive organs. (9) Subjects with some kind of drug and/or food allergy. (10) Subjects who are now under another clinical study with a medicine/food, or took part in that within 4 weeks before this study, or will join that after giving informed consent to join this study. (11) Subjects who donated over 200 mL of their whole blood and/or blood components within a month before this study. (12) Subjects who donated over 400 mL of their whole blood within the last 4 months before this study. (13) Subjects who will be collected over 800 mL in total of their blood within 12 months, before and in this study. (14) Subjects who have been determined as ineligible for participation, by the principal/sub investigator's opinions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method