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A study to evaluate the effect of decreasing cholesterol level by ingestion of botanical ingredient-containing foods.

Not Applicable
Conditions
ot applicable
Registration Number
JPRN-UMIN000022940
Lead Sponsor
Suntory Business Expert Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
200
Inclusion Criteria

Not provided

Exclusion Criteria

1) Females in pregnancy, lactation and scheduled pregnancy period. 2) Subjects who are attending other studies or attended other studies within past 4 weeks. 3) Subject who are receiving continuous medical treatment. 4) Subjects who are; (a) With present heart disorder, liver disorder, or kidney disorder, (b) With previous or present cardiac disorder, (c) With diabetes mellitus, or (d) With allergy to the study foods. 5) Subjects who are deemed to be unsuitable by the investigator.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
DL cholesterol level, 4, 8 and 12 weeks after investigation.
Secondary Outcome Measures
NameTimeMethod
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