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Curcumin Supplement
Treatment3 for Healthy Subjects (CRC Trial)
N/A
Waitlist Available
Led By Britt M Burton-Freeman, Ph.D
Research Sponsored by Clinical Nutrition Research Center, Illinois Institute of Technology
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 hours postprandial study
Awards & highlights
CRC Trial Summary
This trial will compare 2 different capsule formulations of curcumin to unformulated Curcuma longa extract in terms of curcumonoid metabolite absorption and relative bioavailability.
CRC Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 8 hours postprandial study
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 hours postprandial study
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in plasma curcumin metabolites among 3 different treatments
Secondary outcome measures
Changes in urine metabolites among 3 different treatments
CRC Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Treatment3Experimental Treatment1 Intervention
Curcuma longa extract of Rhizomes
Group II: Treatment 2Active Control1 Intervention
Longvida Capsule formulation B
Group III: Treatment1Active Control1 Intervention
Longvida Capsule formulation A
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Treatment3
2017
N/A
~10
Find a Location
Who is running the clinical trial?
Verdure SciencesIndustry Sponsor
4 Previous Clinical Trials
77 Total Patients Enrolled
Clinical Nutrition Research Center, Illinois Institute of TechnologyLead Sponsor
53 Previous Clinical Trials
2,911 Total Patients Enrolled
Britt M Burton-Freeman, Ph.DPrincipal InvestigatorIllinois Institute of Technology
3 Previous Clinical Trials
150 Total Patients Enrolled
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