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Clinical Trials/JPRN-UMIN000014115
JPRN-UMIN000014115
Completed
未知

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

KSO Corporation0 sites90 target enrollmentMay 30, 2014

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
KSO Corporation
Enrollment
90
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
May 30, 2014
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Not specified

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