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Verification study on the effect of food material intake on abdominal visceral fat-Randomized, double-blind, placebo-controlled parallel group study-

Verification study on the effect of food material intake on abdominal visceral fat-Randomized, double-blind, placebo-controlled parallel group study- - Verification study on the effect of food material intake on abdominal visceral fat

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000044727
Enrollment
90
Registered
2021-07-02
Start date
2021-08-17
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

None listed

Interventions

Sponsors

Maruzen Pharmaceuticals Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Japanese Males and females aged of 20-64 years 2)Subjects with BMI >=23 kg/m2 and <30 kg/m2 3)Subjects who can visit on schedule days 4)Subjects who recognize the object and contents of the study and submit the written informed consent

Exclusion criteria

Exclusion criteria: 1)Subjects who are under treatment or have a history of severe illness in the heart, liver, kidney, digestive organs or other organs 2)Subjects who dyslipidemia, high blood pressure, or diabetes 3)Subjects who received medication treatment or surgery due to serious illness or injury within 1 month from the start of this study 4)Subjects who regularly use health foods and supplements affecting the study 5)Possible pregnancy, pregnancy and lactation 6)Heavy drinkers 7)Subjects who feel bad mood by blood collect 8)Subjects 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 9)Those who have been diagnosed with chronic constipation 10)Shift worker 11)Subjects who plan business trip or trip for 10 days or more a month 12)Subjects who have allergy related to the test foods 13)Subjects already participating in other clinical trials 14)Subjects who are ineligible due to physician's judgment

Design outcomes

Primary

MeasureTime frame
Visceral fat area

Secondary

MeasureTime frame
Body weight,BMI,Waist circumference,hip circumference, W/H ratio,Subcutaneous fat area,total fat area,total cholesterol,LDL- cholesterol,HDL- cholesterol,triglyceride,glucose,HbA1c

Countries

Japan

Contacts

Public ContactTomoya Yuhki

New drug research center, Inc. Clinical Research Dept.

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

Outcome results

None listed

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