JPRN-UMIN000027767
Completed
未知
A clinical study for evaluating the efficacy of seasoning containing functional ingredients on the suppression of the elevation of postprandial serum triglyceride. (Randomised, placebo controlled crossover study) - A clinical study for evaluating the efficacy of seasoning containing functional ingredients on the suppression of the elevation of postprandial serum triglyceride.
CPCC Company, Limited0 sites16 target enrollmentJune 21, 2017
ConditionsHealthy adult
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy adult
- Sponsor
- CPCC Company, Limited
- Enrollment
- 16
- 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 use oral medication, supplements and/or functional foods affecting lipid metabolism (2\) Individuals who are pregnant or breast\-feeding, or have the will of pregnancy during the study period. (3\) Individuals who are suffered from or under treatment of serious disease (e.g., heart disease, liver disease, kidney disease, and/or digestive disease) (4\) Individuals who are under treatment of alcohol dependence (5\) Individuals who are extremely irregular in eating habits (6\) Individuals who declare the allergy symptoms against drugs and/or foods (7\) Individuals who are participating in other clinical trials of drugs or health food, who participated in the last 4 weeks, or who are willing to participate after giving the informed consent. (8\) Individuals who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study (9\) Males who have donated over 400 mL of blood and/or blood component within the last three months prior to the current study (10\) Females who have donated over 400 mL of blood and/or blood component within the last four months prior to the current study (11\) Males whose total blood collection volume exceeding 1200 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (12\) Females whose total blood collection volume exceeding 800 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (13\) Individuals who are judged as unsuitable for the study by the investigator for the other reasons
Outcomes
Primary Outcomes
Not specified
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