Status:
COMPLETED
Theracurmin vs Curcumin Bioavailability Study
Lead Sponsor:
Handok Inc.
Conditions:
Bioavailability
Eligibility:
All Genders
19-60 years
Phase:
NA
Brief Summary
A randomized, open-label, cross-over, single administration study to compare bioavailability of curcumin in health adults
Detailed Description
* Randomization, Open-label, 3-period, 6-sequence, Crossover, Single * Drug-free inverval : more than 7 days * Sampling time : 0,0.5,1,1.5,2,3,4,6,8,12h
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Healthy adult 19 to 60 years
- BMI 18.0\~30.0kg/m2 at screening
- Subject who was given, and fully understood, the information about the study, and has provided voluntary written informed consent to participate in the study and agreed to comply with the study requirements.
- Exclusion Criteria
- A person with clinically significant disease corresponding to cardiovascular, respiratory, liver, kidney, digestive system, blood/tumor system, endocrine system, immune system, neuropsychiatry or who has a history within the last 6 months.
- A person with a history of gastrointestinal disease or surgery (except for simple cecal surgery or hernia surgery) that may affect the absorption of food for clinical research.
- Persons who have an irritable reaction to foods containing turmeric or other drugs and food.
- Those who took medicines within 7 days before the first intake of food for clinical research.
- Food for Clinical Research If you have consumed foods containing turmeric (eg, radishes, curry) within 7 days before the first intake of food, or you can't consume until the day of intake of food for the last clinical study.
- Those who have participated in other clinical studies within 90 days prior to the first intake of food for clinical research.
- Women who are pregnant or lactating during screening, or who plan to become pregnant during clinical research. A person who is deemed unsuitable for participating in this clinical study because of other reasons.
Exclusion
Key Trial Info
Start Date :
July 31 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 29 2019
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT04028739
Start Date
July 31 2019
End Date
November 29 2019
Last Update
December 6 2019
Active Locations (1)
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1
Korea Kuro Hospital
Seoul, South Korea