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Human safety test of Macaranga tanarius fruit extract

Human safety test of Macaranga tanarius fruit extract - Human safety test of Macaranga tanarius fruit extract

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000059713
Enrollment
30
Registered
2025-11-10
Start date
2025-09-08
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 adult

Interventions

The test product will be a No. 2 hard capsule (made of hydroxypropyl methylcellulose) containing 100 mg of Macaranga tanarius fruit extract. The administration period will generally be four weeks, an

Sponsors

Southen Knights' Laboratory Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Basically, healthy men and women aged 20 to 65

Exclusion criteria

Exclusion criteria: Participants who meet any of the following criteria will be excluded. 1) Participants currently receiving treatment for or have a history of malignant tumors, heart failure, or myocardial infarction. 2) Participants with a pacemaker or implantable cardioverter-defibrillator. 3) Participants currently receiving treatment for the following chronic diseases: arrhythmia, liver damage, chronic kidney disease, cerebrovascular disease, rheumatic disease, diabetes, dyslipidemia, hypertension, cardiovascular disease, and other chronic diseases. 4) Participants currently taking foods for specified health uses or foods with functional claims. 5) Participants currently taking or using medicines (including herbal medicines) or supplements. 6) Participants with allergies (to medicines or foods related to the test food). 7) Participants currently pregnant, breastfeeding, or intending to become pregnant during the study period. 8) Participants who have participated in other clinical trials within the 28 days prior to the consent acquisition date, or who plan to participate in such trials during the study period. 9) Participants deemed inappropriate for this study by the investigator.

Design outcomes

Primary

MeasureTime frame
General blood tests and blood biochemistry tests

Countries

Japan

Contacts

Public ContactKimio Sugaya

Southen Knights' Laboratory Co., Ltd. Representative Director

sugaya0822@yahoo.co.jp09049987459

Outcome results

None listed

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