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Effect of Curcumin on Iron Metabolism in Healthy Volunteer

Effect of Curcumin on Iron Metabolism in Healthy Volunteer

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01489592
Acronym
CURHEP
Enrollment
18
Registered
2011-12-09
Start date
2011-10-31
Completion date
2012-03-31
Last updated
2025-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Volunteers

Brief summary

The purpose of this study is to determine the impact of curcumin, administrated orally, on iron metabolism in healthy volunteers. Iron metabolism will be describe by hepcidin expression that the investigators observed in vitro and serum hepcidin levels.

Interventions

oral administration of 6 grams of curcumin

Sponsors

Institut National de la Santé Et de la Recherche Médicale, France
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Body mass index between 18 et 25 Kg/m² * Non smoker * No swallowing disorders * Normal clinical exam * Normal ECG * Normal values for routine biological tests : serum iron, transferrin saturation,, hemogram ferritin, C Reactive Protein, AST, ALT, HDL and LDL cholesterol, triglycerides * No C282Y mutation within the HFE gene * Affiliation to social security * Written informed consent obtained

Exclusion criteria

* Chronic or evolutive disease * Infection during the 7 days before each sequence * Drug or alcohol (\>30g) abuse * Current treatment * Known food allergy * stay at altitude (\> 1500m) in 2 months * Positive serology for hepatitis B or C virus or HIV. * Transfusion or blood donation during the last three months. * Exclusion period on the healthy volunteer National File.

Design outcomes

Primary

MeasureTime frame
Maximal variation of serum hepcidin level after oral administration of curcuminwithin 48 hours after administration of curcumin

Secondary

MeasureTime frameDescription
Plasmatic iron bioavailability30min, 1H, 2H, 3H, 4H, 6H, 8H, 12H, 24H et 48HIron, ferritin, transferrin, transferrin saturation
Evaluation of the inhibitory activity of volunteers's serum on hepcidin expression by hepatocytes30min, 1h, 2h, 3h, 4h, 6h, 8h, 12h, 24hIn vitro: * the coculture model that we previously developed to analyze endogenous hepcidin expression, and * human hepatic cells line (HepG2) stimulated or not by IL-6 which governs the STAT3 pathway, transfected with gene reporter constructs containing hepcidin promoter.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026