JPRN-UMIN000045502
Completed
未知
A study on the effect of single intake of the test food on blood sugar-related biological markers -a placebo-controlled, double-blind, four-period crossover trial- - A study on the effect of single intake of the test food on blood sugar-related biological markers
IMEQRD Co., Ltd0 sites10 target enrollmentOctober 8, 2022
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- IMEQRD Co., Ltd
- Enrollment
- 10
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •1\. Individuals who currently have been taking any medication drugs or Chinese herbal medicines for medical treatments. (Single dose to be taken only once is approved.) 2\. Individuals who have severe diseases or a history of severe diseases, such as cardiac\-, hepatic\-, kidney\-, and digestive\- diseases. 3\. Individuals who are managed by medical doctors for diet therapy and exercise therapy. 4\. Individuals who have currently been taking commercially available drugs, quasi\-drug products, and foods or supplements with functional claims which affect blood sugar levels. (However, individuals who can discontinue taking these materials during the trial period after obtaining informed consent will be allowed to join the trial.) 5\. Individuals who drink more than 60 g alcohol/day. 6\. Individuals who live irregular life rhythms, such as work in shift, night shift, and marked irregular eating habits. 7\. Individuals who joined other clinical trials from 1 month before obtaining informed consent in this trial, or those who have currently been joined other clinical trials. Also, those who are planning to join other clinical trials between 4 weeks after this trial. 8\. Individuals who can't stop drinking one day before the experimental day. 9\. Individuals who have drug allergies and food allergies. 10\. Individuals who are unsuitable for this trial, that judged by the principal investigator.
Outcomes
Primary Outcomes
Not specified
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