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Pharmacokinetic analysis of novel curcumin preparation in health volunteer

Pharmacokinetic analysis of novel curcumin preparation in health volunteer - Pharmacokinetic analysis of novel curcumin preparation in health volunteer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039083
Enrollment
12
Registered
2020-01-08
Start date
2019-12-18
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy volunteer

Interventions

Intervention, group A Novel curcumin preparation 1 90mg/day for 1 day A washout period for 1 weeks Novel curcumin preparation 2 90mg/day for 1 day A washout period for 1 weeks Theracurmin 90mg/

Sponsors

University of Shizuoka
Lead Sponsor
Therabiopharma ltd.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The healthy volunteers

Exclusion criteria

Exclusion criteria: 1) The person with underlying disease 2) Pregnancy and nursing 3) Cognitive impairment 4) The person who uses the supplement which influence stiff shoulder 5) The person who participates in other clinical trials at the time of this study entry 6) etc

Design outcomes

Primary

MeasureTime frame
Serum curcumin concentration AUC Cmax

Countries

Japan

Contacts

Public ContactYoichi Sunagawa

University of Shizuoka Division of Molecular Medicine, School of Pharmaceutical Sciences

y.sunagawa@u-shizuoka-ken.ac.jp0542645765

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026