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A study to evaluate the effects of plant extract material on blood lipid parameters

A study to evaluate the effects of plant extract material on blood lipid parameters - A study to evaluate the effects of plant extract material on blood lipid parameters

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000046571
Enrollment
72
Registered
2022-01-08
Start date
2022-01-08
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 volunteers

Interventions

Sponsors

Soiken Inc.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Healthy males and females whose age of 40 years or more and less than 65 years 2) Subject whose BMI is 23.0 kg/m2 or more and less than 30.0 kg/m2 3) Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study and being able to personally sign a written informed consent

Exclusion criteria

Exclusion criteria: 1) Subjects with serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2) Subjects who take regularly pharmaceuticals or quasi-drugs which may affect lipid metabolism , such as lipid-lowering drugs or antihypertensive drugs, etc. 3) Subjects who take regularly Foods for Specified Health Uses or Foods with Function Claims labeled the functions related to lipid disorders or blood pressure 4) Subjects who have the possibility of developing allergic symptoms by the test food 5) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 6) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 7) Subjects who took part in another study within 3 months prior to the start of the present study or who is currently taking part in another study 8) Subjects deemed unsuitable by the investigator

Design outcomes

Primary

MeasureTime frame
LOX-index(sLOX-1, LAB)

Secondary

MeasureTime frame
body weight, BMI, blood test, VAS(fatigue sensation)

Countries

Japan

Contacts

Public ContactKota Watanabe

Soiken Inc. R&D Division

watanabe_kota@soiken.com06-6871-8888

Outcome results

None listed

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