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Body fat-reducing effect of tablets containing lactoferrin and cacao extract: A randomized, double-blind, placebo-controlled, parallel-group study

Body fat-reducing effect of tablets containing lactoferrin and cacao extract: A randomized, double-blind, placebo-controlled, parallel-group study - Body fat-reducing effect of tablets containing lactoferrin and cacao extract

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016239
Enrollment
60
Registered
2015-01-16
Start date
2015-01-18
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

No (healthy adults or slightly overweight subjects)

Interventions

Ingestion of 4 tablets containing lactoferrin and cacao extract once a day for 12 weeks Ingestion of 4 tablets not containing lactoferrin and cacao extract once a day for 12 weeks

Sponsors

KSO Corporation
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males and females aged 20 to 64 years old. (2) Subjects have three square meals a day. (3) Subjects whose BMI are 23 to 24.9 or 25 to 29.9. (4) Subjects with visceral fat areas of more than 80 cm2 (on CT analysis) at the screening test. (5) Subjects giving written informed consent.

Exclusion criteria

Exclusion criteria: (1) Subjects who use medications affecting obesity, hyperlipidemia, lipid metabolism, and so on. (2) Subjects who can't stop using supplements and/or functional foods affecting obesity, hyperlipidemia, lipid metabolism, and so on. (3) Subjects who are pregnant or lactating. (4) Subjects who have under treatment or a history of drug addiction and/or alcoholism. (5) Subjects who are planned to participate in other clinical study. (6) Subjects who are judged as unsuitable for the study by the investigator for the other reason.

Design outcomes

Primary

MeasureTime frame
1) Visceral fat area 2) Total fat area 3) Subcutaneous fat area measured before and 12 weeks after ingestion of the tablets.

Countries

Japan

Contacts

Public ContactYoshika Komori

KSO Corporation Sales department

yoshi@kso.co.jp03-3452-7733

Outcome results

None listed

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