A human study to evaluate safety and effectiveness of Perilla oil on blood flow
- Conditions
- Not Applicable
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
1) Man and women (19 years = Age < 70 years)
2) Smoker
1) Volunteer who has taken drugs or healthy functional food affecting lipid metabolism, platelet function, or coagulation reactions within a month before the first visit.
2) Following diseases :
Dyslipidemia, platelet dysfunction, etc.
3) Volunteer who consumes a large amount of foods rich in omega-3 fatty acids.
4) Volunteer who has recently experienced a weight change or is on a diet for weight control.
5) Excessive exercise
6) Volunteer who drink continuously
7) Volunteer who has been in clinical demonstration within 1 month
8) Pregnant woman, lactating women or planning to pregnant
9) Volunteer who are hypersensitivity or allergy to dietary supplement or ingredients contained in the supplement.
10) Volunteer who judged incongruent by tester through clinical examination center
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Platelet aggregation, blood coagulation, fibrinolysis, blood lipid profile
- Secondary Outcome Measures
Name Time Method Adverse reaction, vital signs