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A human trial to evaluated the absorption rate of curcumin for Hydrocumin in Health Human Volunteers

A human trial to evaluated the absorption rate of curcumin for Hydrocumin in Health Human Volunteers

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0009850
Enrollment
20
Registered
2024-10-16
Start date
2023-07-15
Completion date
Unknown
Last updated
2024-11-14

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

Conditions

None listed

Interventions

Dietary Supplement : • HydroCumin group: 1 tube once, single-dose, with water(300 mL){8g, 400 mg for curcuma longa L. extract(curcumin)} • Curcumin group:1 tube once, single-dose, with water(300 mL){8

Sponsors

Wonkwang University Oriental Medical Hospital, Jeonju
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) healthy male aged 19 years-39 years at the screening test 2) BMI 17.5-29.9 kg/m^2 and weight 55 kg or more 3) Spontaneously agreed to participate in the study by the patients and legal guardians or parents

Exclusion criteria

Exclusion criteria: 1) Participants with a clinically significant disease requiring treatment (i.e., acute or chronic cardiovascular system, endocrine system, immune system, respiratory system, kidney and urinary system, neuropsychiatric system, musculoskeletal inflammation, inflammatory disease, blood and tumor disease, gastrointestinal disease, etc.) 2) Participants with a history of antipsychotic medication use within 3 months prior to the screening examination 3) Those who have or are suspected of alcohol or drug abuse 4) Those who participated in other human tirals within 2 months before the screening test 5) Patients who have laboratory test outcomes as follow ? AST(Aspartate aminotransferase), ALT(Alanine Transaminase) > three times the normal limit ? Serum Creatinine > 1.5 mg/dL 6) Patients who are judged ineligible to participate in the trial by the principal investigator for other reasons, including laboratory test outcomes.

Design outcomes

Primary

MeasureTime frame
density of curcumin

Secondary

MeasureTime frame
AUC, Cmax, Tmax, RB

Countries

Korea, Republic of

Contacts

Public ContactJoo Jongcheon

Wonkwang University Oriental Medical Hospital, Jeonju

jcjoo2000@hanmail.net+82-63-270-1073

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026