A study to check the bioavailability of one drug compare to the other drug in healthy volunteers.
- Registration Number
- CTRI/2014/08/004897
- Lead Sponsor
- Akay Flavours Aromatics PvtLtd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
1. Healthy volunteers of age 20 to 55 years of either sex who are not involved in any regular medication or supplementation.
2. Subjects who are willing to give their written informed consent and comply with the protocol requirements.
1. Patient who took turmeric contained food 2 days prior to screening
2. Pregnant or lactating women.
3. Subjects with known hypersensitivity to the investigational products.
4. Subjects who have participated in any clinical trial in the past 1 month.
5. Any subjects found to have entered in to the study in violation of this protocol or if the subject is uncooperative during the study.
6. Any other condition that in the opinion of the investigator that does not justify the subjectâ??s participation in the trial
Study & Design
- Study Type
- BA/BE
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Curcuminoids in bloodTimepoint: 24 Hours
- Secondary Outcome Measures
Name Time Method Time of presence of curcuminoids in bloodTimepoint: 24 Hours