Eligibility Module

Eligibility Module

The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.

Eligibility Module path is as follows:

Study -> Protocol Section -> Eligibility Module

Eligibility Module


Ignite Creation Date: 2025-12-24 @ 9:15 PM
Ignite Modification Date: 2025-12-24 @ 9:15 PM
NCT ID: NCT05349604
Eligibility Criteria: Inclusion Criteria: 1. Healthy adults 19 years of age or older as of the screening date 2. Those with no history of treatment for hypertension within the last 3 months 3. A person who voluntarily decides to participate and agrees in writing to abide by the precautions after hearing and fully understanding the detailed explanation of this study Exclusion Criteria: 1. Those with systolic blood pressure of 160 mmHg or higher or diastolic blood pressure of 100 mmHg or higher 2. Those who have had a stroke, myocardial infarction, percutaneous coronary angioplasty or surgery for coronary angioplasty within the past 6 months 3. Persons with acute and severe cardiovascular diseases such as heart failure, myocardial infarction, and stroke 4. Those with acute/chronic inflammation such as cancer, rheumatic disease, autoimmune disease, gastrointestinal disease, etc. 5. Those who have a history of gastrointestinal diseases (eg Crohn's disease) or gastrointestinal surgery (except simple appendicectomy or hernia surgery) that may affect the absorption of the product for human application testing 6. Persons who have taken prohibited concomitant drugs within the last 3 months 7. Persons with a history of clinically significant hypersensitivity reactions to drugs and health functional foods 8. Those who have received antipsychotic drug treatment within 2 months before the screening test 9. Persons with a history of drug or alcohol abuse 10. Pregnant or lactating women 11. When women of childbearing potential of childbearing potential do not accept the implementation of appropriate contraceptive methods (except for women who have undergone sterilization) 12. Subjects who have participated in health functional food related research or clinical trials within the last 3 months 13. In case the principal investigator judges that it is not appropriate to participate in this study
Healthy Volunteers: True
Sex: ALL
Minimum Age: 19 Years
Study: NCT05349604
Study Brief:
Protocol Section: NCT05349604