Skip to content

Study of effects of food containing Fucoidan on LDL-cholesterol, Blood glucose, Triglyceride.

Study of effects of food containing Fucoidan on LDL-cholesterol, Blood glucose, Triglyceride. - Study of effects of food containing Fucoidan on LDL-cholesterol, Blood glucose, Triglyceride.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018029
Enrollment
40
Registered
2015-06-26
Start date
2015-06-29
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

Sponsors

TTC Co.,Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males and females from 20 to 64 years of age (2) Subjects falling under any of the following 1. LDL-Cholesterol level is greater or equal to 120 mg/dL 2. Fasting blood glucose level is greater or equal to 100 mg/dL 3. Serum Triglyceride level is greater or equal to 150 mg/dL

Exclusion criteria

Exclusion criteria: (1) Subjects who routinely use health food containing Fucoidan (2) Subjects who constantly use oral medication and/or functional foods affecting body fat, serum lipid levels, lipid metabolism and/or glycometabolism (3) Subjects who has disease requiring regular medication or receiving treatment or needing treatment (4) Subjects who has under treatment or a history of serious disease(e.g., diabetes, liver disease, kidney disease, or heart disease) (5) Subjects judged as unsuitable for this study based on the results of clinical examination or cardiopulmonary abnormality (6) Subjects with allergies to the products used in the study (7) Subjects who are judged as unsuitable for the study based on the results of clinical and physical examination on preliminary examination (8) Subjects who intend to become pregnant or lactating (9) 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 (10) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (11) Subjects judged as unsuitable for the study by the investigator for other reasons

Design outcomes

Primary

MeasureTime frame
LDL-cholesterol Blood glucose Triglyceride Total-cholesterol HDL-cholesterol HbA1c Adverse event

Countries

Japan

Contacts

Public ContactYuki Kitahara

TTC Co.,Ltd. Clinical Research Planning Department

y.kitahara@ttc-tokyo.co.jp03-5459-5329

Outcome results

None listed

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