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Suppressive effect of test food on postprandial serum triglyceride level

Suppressive effect of test food on postprandial serum triglyceride level - Suppressive effect of test food on postprandial serum triglyceride level

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000027893
Enrollment
60
Registered
2017-06-26
Start date
2017-06-26
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 adults

Interventions

The capsule containing kiwi fruit extract intake - Washout - Placebo intake Placebo intake - Washout - The capsule containing kiwi fruit extract intake

Sponsors

CPCC Co.,Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Healthy subjects aged 20 to 59 years old (2) BMI < 25 (3) Subjects whose fasting serum triglyceride level is <= 150 mg/dL (4) Subjects who agree to participate in the current study with written informed consent

Exclusion criteria

Exclusion criteria: (1) Subjects who use oral medication, supplements and/or functional foods affecting lipid metabolism (2) Subjects who are pregnant or breast-feeding, or have the will of pregnancy during the study period (3) Subjects who are suffered from or under treatment of serious disease (e.g., heart disease, liver disease, kidney disease, and/or digestive disease) (4) Subjects who are under treatment of alcohol dependence (5) Subjects who are extremely irregular in eating habits (6) Subjects who declare the allergy symptoms against drugs and/or foods (7) Subjects who are participating in other clinical trials of drugs or health food, who participated in the last 4 weeks, or who are willing to participate after giving the informed consent (8) Subjects who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study (9) Males who have donated over 400 mL of blood and/or blood component within the last three months prior to the current study (10) Females who have donated over 400 mL of blood and/or blood component within the last four months prior to the current study (11) Males whose total blood collection volume exceeding 1200 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (12) Females whose total blood collection volume exceeding 800 mL within the last twelve months prior to the current study (include the blood collection volume of the current study) (13) Subjects who are predicted to be difficult to comply with agreements and subject management (14) Subjects who are judged as unsuitable for the study by the investigator for the other reasons

Design outcomes

Primary

MeasureTime frame
Time course of delta AUC (area under the curve) and delta serum triglyceride level

Secondary

MeasureTime frame
Time course of AUC (area under the curve) and serum triglyceride level

Countries

Japan

Contacts

Public ContactSatomi Iwata

Omnica Co.,Ltd. Research and Development Dept.

iwata@omnica.co.jp03-5840-9815

Outcome results

None listed

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