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NCT05349032 Clinical Trial

Assessing the Bioavailability of Leading Phytonutrient Products

Inflammation Clinical Trial

Official title:
Assessing the Bioavailability of Leading Phytonutrient Products

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05349032
Other study ID # 101
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date June 2022

Study information
Verified date April 2022
Source Epiceutical Labs
Contact David Roberts, MPH
Phone 810777687
Email research@epiceuticallabs.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will primarily test various phytonutrient-based supplements to see which gets absorbed into the body the best. The study will secondarily look at inflammatory markers in the urine to determine any change.

Description:

This study will primarily test various phytonutrient-based supplements to see which gets absorbed into the body the best. 120 mg of curcumin from brands Meriva, CurcElite, Lonvida, UltraCur, NovaSol. The study will secondarily look at inflammatory markers in the urine to determine any change.

Recruitment information / eligibility
Status Recruiting
Enrollment 15
Est. completion date June 2022
Est. primary completion date April 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 21 Years to 49 Years
Eligibility Inclusion Criteria: - Age and gender Exclusion Criteria: - Cannot take any phytonutrient or curcumin supplement five days prior to commencement.

Study Design

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• Curcumin
Oral supplement

Locations
Country Name City State
United States David Roberts Charlottesville Virginia

Sponsors (1)
Lead Sponsor Collaborator
Epiceutical Labs

Country where clinical trial is conducted

United States, 

References & Publications (1)

Jamwal R. Bioavailable curcumin formulations: A review of pharmacokinetic studies in healthy volunteers. J Integr Med. 2018 Nov;16(6):367-374. doi: 10.1016/j.joim.2018.07.001. Epub 2018 Jul 4. Review. Erratum in: J Integr Med. 2019 Jul;17(4):310. — View Citation

Outcome
Type Measure Description Time frame Safety issue
Primary Bioavailability Blood Plasma 0, 1, 2, 4, and 12 hours
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