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Study on evaluation of reduction effect of test supplement on body fat -a randomized, double blind, placebo controlled, parallel group comparison study-

Study on evaluation of reduction effect of test supplement on body fat -a randomized, double blind, placebo controlled, parallel group comparison study- - Body fat reduction effect of test supplement

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000037062
Enrollment
100
Registered
2019-06-14
Start date
2019-06-14
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 subject

Interventions

Sponsors

TTC Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Japanese male and female whose age is between 45 and 70 years old 2. Subjects whose BMI is between 23 and 30

Exclusion criteria

Exclusion criteria: 1. Subjects who are currently under medical treatment, diet therapy or exercise therapy. 2. Subjects who are under treatment or have a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease, abnormal secretion disease of adrenocortical hormone) 3. Subjects with allergies to the test food in this study 4. Females who are known or suspected to be pregnant, breastfeeding or desire to become pregnant during the trial period. 5. Subjects who routinely use some medicine, health foods affecting body fat or lipid metabolism. 6. Subjects who currently are dieting. 7. Subjects who have participated in other clinical study within the past month prior. 8. Subjects who use some medicine, food containing lactic acid bacteria or polymethoxyflavone 3 days a week or more from half a year before the informed consent. 9. Subjects who are judges as unsuitable for the study based on the results of lifestyle questionnaire 10. Subjects who are judged as unsuitable for the study based on the results of clinical laboratory test or cardiopulmonary function. 11. Subjects who have diseases requiring continuous medication, or serious medical history who needed medication therapy 12. Subjects who always use laxative when defecation. 13. Subjects who have taken antibiotics within the past month 14. Subjects who are judged as unsuitable for the study based on the results of clinical laboratory test or physical examination. 15. Subjects who are planning to travel abroad during the study period, or who are planning of long term domestic trip for more than one week in study period. 16. Subjects who are judged as unsuitable for the study by the investigator for other reason

Design outcomes

Primary

MeasureTime frame
Abdominal visceral fat area

Secondary

MeasureTime frame
Abdominal total fat area, abdominal subcutaneous fat area, body weight, BMI, waist circumference, hip circumference, ratio of waist and hip circumferences, subgroup analysis (BMI, abdominal visceral fat area, sex, defecation frequency)

Countries

Japan

Contacts

Public ContactShingo Yamamichi

TTC Co., Ltd. Clinical Research Planning Department

s.yamamichi@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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