A study for evaluating the effect of the intake of an indigestible dextrin-containing beverage on postprandial increase in Serum Triglyceride : randomized, placebo-controlled, double blind cross-over trial
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000017824
- Lead Sponsor
- TTC Co.,Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 90
Not provided
(1) Subjects who routinely use food containing of indigestible dextrin (2) Subjects routinely taking medicine or health food which may influence lipid metabolism (3) Subjects who are under medication or having a history of serious diseases for which medication was required (4) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (5) Subjects having possibilities for emerging allergy related to the study (6) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (7) Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study (8) Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating (9) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (10) Subjects judged as unsuitable for the study by the investigator for other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method area under the curve for serum triglyceride levels
- Secondary Outcome Measures
Name Time Method fasting triglyceride level, triglyceride level of 2,3,4 and 6hours after the high-fat meal ingestion, Remnant-like particle cholesterol