Examination of the Effects of Long Pepper Extract on Blood Flow and Skin Surface Temperature Following the Exposure to Cold Water Stress: Placebo controlled, Randomized, Double-blind, Cross-over Study
- Conditions
- /A (healthy adults)
- Registration Number
- JPRN-UMIN000025893
- Lead Sponsor
- TES Holdings Co., Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Female
- Target Recruitment
- 30
Not provided
[1]Individuals using medical products. [2]Individuals who used a drug to treat a disease in the past 1 month (except temporal usage for pollenosis). [3]Individuals who use a drug to treat a disease. [4]Individuals who were an asthmatic patient in the past 3 months or is an asthmatic patient. [5]Individuals with serious anemia. [6]Individuals who are sensitive to a test product or other foods, and medical products. [7]Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplements in the past 3 months or will ingest those foods during the test period. [8]Individuals with serious diseases (ex. diabetes, hepatopathy disease, kidney damage, heat failure, endocrine disease), or who are a patient of or have a history of thyroid disease, adrenal disease, metabolic disease). [9]Individuals who conducted hormone replacement therapy in the past 3 months or have a history of conducting hormone replacement therapy. [10]Individuals who have an inflammation or a scar on a measuring area. [11]Individuals whose systolic blood pressure is over 160mmHg or diastolic pressure is over 100mmHg. [12]Individuals who excessively take alcohol (expressed in an amount of alcohol: over 60mg/day). [13]Individuals who donated blood over 200mL in the past 1 month or over 400mL in the past 3 months. [14]Individuals who are a smoker. [15]Individuals who participated in other clinical studies in the past 3 months. [16]Individuals whose Simplified Menopausal Index score is over 51. [17]Individuals who have a history of ovarian resection or hysterectomy. [18]Individuals who are or are possibly, or are lactating. [19]Individuals judged inappropriate for the study by the principal.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method