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Study of Effect of Food Containing Resistant Maltodextrin on Postprandial Serum Triglyceride

Not Applicable
Conditions
o (subjects with high postprandial serum triglyceride)
Registration Number
JPRN-UMIN000014115
Lead Sponsor
KSO Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
90
Inclusion Criteria

Not provided

Exclusion Criteria

(1)Subjects who use oral medication affecting lipid metabolism. (2)Subjects who constantly use supplements and/or functional foods affecting lipid metabolism. (3)Subjects with excessive alcohol-drinking behaviors. (4)Subjects who can't stop drinking for 2 days until the screening checkup (5)Subjects who declare the allergy symptoms against high-fat diets. (6)Subjects who have a history of serious disease (e.g., diabetes, liver disease, kidney disease, and/or heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder. (7)Subjects who have a chronic disease and use medicines continuously. (8)Subjects who have a history of digestive disease affecting digestion and absorption. (9)Subjects who are judged as unsuitable for the study based on the results of blood test. (10)Subjects who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study or over 400 mL of blood and/or blood component within the last three months prior to the current study. (11)Subjects who is diagnosed as familial hyperlipidemia. (12)Subjects who is diagnosed as severe anemia and not suitable for frequent collection of blood. (13)Subjects who have under treatment or a history of drug addiction and/or alcoholism. (14)Subjects who are planned to participate in other clinical study. (15)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (16)Subjects who are judged as unsuitable for the study by the investigator for other reason.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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