A clinical study for the effects of a plant extract on improving vascular endothelial function - Randomized, double-blind, placebo-controlled parallel-group comparative study
- Conditions
- Healthy Individuals
- Registration Number
- JPRN-UMIN000038722
- Lead Sponsor
- Ezaki Glico Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 54
Not provided
(1) Subjects who have received some kind of treatment or care at the time of study participation. (2)Subjects who are during pregnancy or lactation, and intend to be pregnant during the study period. (3)Subjects who have a smoking habit (4)Subjects having blood sample of 200 mL within 4 week at the start of this study. (5)Subjects having blood sample of 400 mL within 16 week at the start of this study. (6)Subjects having blood sample of 1000 mL or more than within 48 hours at the start of intake of test food. (7)Subject in other clinical trials or trials. (8)Subjects who fall under any of the following items. a. Subjects who have heart, liver, or kidney disease (including complications of other diseases) b.Subjects with a history of cardiovascular disease. c.Subjects who have diabetes. d. Subjects with or having a history of serious diseases such as cancer and asthma. (9)Subjects who have a history of major surgery in the gastrointestinal tract such as gastrectomy, gastrointestinal suture, and intestinal resection. (10)Subjects who have severe food allergies. (11)Subjects who regularly use supplements, vegetable juice, and tomato juice that have the same ingredients as the test food. (12)Subjects who cannot refrain from taking Citrus unshiu during the test period (including the pre-observation period). (13)Subjects determined to be inappropriate by the investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method