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Investigation of the effects of Peucedanum japonicum root extract on lipid metabolism -Randomized, placebo-controlled, double-blind crossover study-

Investigation of the effects of Peucedanum japonicum root extract on lipid metabolism -Randomized, placebo-controlled, double-blind crossover study- - Investigation of the effects of Peucedanum japonicum root extract on lipid metabolism

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055344
Enrollment
10
Registered
2025-07-01
Start date
2024-09-13
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

Intake of placebo food (4 weeks) -&gt
Intake of active food (4 weeks) Intake of active food (4 weeks) -&gt
Intake of placebo food (4 weeks)

Sponsors

Maruzen Pharmaceuticals Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1)Healthy Japanese males aged of 30-49 years 2)Participants whose BMI are 25.0 kg/m2=< and <30.0kg/m2 3)Participants whose body fat ratio are 20%=< 4)Participants who can visit on schedule days 5)Participants who recognize the object and contents of the study and submit the written informed consent

Exclusion criteria

Exclusion criteria: 1)Participants who are under treatment or have a history of severe illness in the heart, liver, kidney, digestive organs or other organs 2)Participants who have been diagnosed or taking medication with dyslipidemia, high blood pressure, or diabetes 3)Participants who received medication treatment or surgery due to serious illness or injury within 1 month from the start of this study 4)Participants who regularly use health foods and supplements affecting the study 5)Heavy drinker (over 40g alcohol/day) 6)Smokers 7)Participants who fasting triglycerides >=200 mg/dL at screening test 8)Participants who feel bad mood by blood collect 9)Participants who donated 200 mL or more of blood within 1 month from the start of the study or subjects who plan to do so during the study period 10)Late-night Shift worker 11)Participants who plan business trip or trip on average more than 10 days per month (excluding Obon vacation and New Year's holidays) 12)Participants who may have allergy symptoms to any of the ingredients contained in the test food or provided food 13)Participants who participated in other clinical studies in the past 3 months or who plan to participate in other clinical studies during the study period 14)Participants who are ineligible due to physician's judgement

Design outcomes

Primary

MeasureTime frame
Blood lipids

Secondary

MeasureTime frame
Blood biochemistry tests

Countries

Japan

Contacts

Public ContactToyotada Ashino

New drug research center, Inc. Clinical Research Dept.

t-ashino@ndrcenter.co.jp0123-34-0412

Outcome results

None listed

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