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A clinical study for evaluating the efficacy of test food on the suppression of the elevation of postprandial serum triglyceride. -Randomised double-blind placebo-controlled trial

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000035337
Lead Sponsor
KSO Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

(1)Individuals who use oral medication affecting lipid metabolism (2)Individuals who constantly use supplements and/or functional foods, including food for specified health use and/or food with function claims, affecting lipid metabolism (3)Individuals who are suffered from or under treatment of serious disease (e.g., diabetes, liver disease, kidney disease, and/or heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder (4)Individuals who have a chronic disease and use medicines continuously (5)Individuals who are diagnosed as severe anemia and not suitable for frequent collection of blood (6)Individuals who had an onset diarrhea within one week from the date of screening, and who is prone to diarrhea always (7)Individuals who are diagnosed as familial hyperlipidemia (8)Individuals who are pregnant or breast-feeding, or have the will of pregnancy during the study period (9)Individuals who are judged as unsuitable for the study by the investigator for the other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time course of serum triglyceride level and AUC (area under the curve)(0-6hrs)
Secondary Outcome Measures
NameTimeMethod
Time course of serum RLP-cholesterol level and AUC (area under the curve)(0-6hrs)
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