A study for evaluating the effect of the intake of a resistant glucan (water-soluble dietary fiber) on postprandial increase in Serum Triglyceride:randomized,placebo-controlled,double blind cross-over trial

A study for evaluating the effect of the intake of a resistant glucan (water-soluble dietary fiber) on postprandial increase in Serum Triglyceride:randomized,placebo-controlled,double blind cross-over trial - A study for evaluating the effect of the intake of a resistant glucan (water-soluble dietary fiber) on postprandial increase in Serum Triglyceride

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000019002

Enrollment

100

Registered

2015-09-14

Start date

2015-09-15

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adult

Interventions

intake of a test food with resistant glucan (single ingestion) - washout period - placebo food without resistant glucan (single ingestion) intake of a placebo food without resistant glucan (single ing

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Males and females from 20 to 64 years of age 2) fasting triglyceride levels are ranged from 120 mg/dL to 199 mg/dL

Exclusion criteria

Exclusion criteria: (1) Subjects who routinely use food rich in dietary fiber (2) Subjects routinely taking medicine or health food which may influence lipid metabolism (3) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (4) Subjects having possibilities for emerging allergy related to the study (5) Subjects who are under medication or having a history of serious diseases for which medication was required (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

Design outcomes

Primary

Measure	Time frame
area under the curve for serum triglyceride levels	—

Secondary

Measure	Time frame
fasting triglyceride level, triglyceride level of 2,3,4 and 6hours after the high-fat meal ingestion, Remnant-like particle cholesterol	—

Countries

Japan

Contacts

Public ContactChiharu Goto

TTC Co.,Ltd. Clinical Research Planning Department

c.goto@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026