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A study to investigate the blood kinetics of food material

Not Applicable
Conditions
Healthy volunteers
Registration Number
JPRN-UMIN000046259
Lead Sponsor
Soiken Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects with serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2) Subjects who go to the hospital with lifestyle-related diseases (high blood pressure, dyslipidemia, diabetes, etc.) 3) Subjects who have the possibility of developing allergic symptoms by the test food 4) Subjects who have the plan to change their lifestyle 5) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 6) Subjects who took part in another study within 3 months prior to the start of the present study or who is currently taking part in another study 7) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 8) Subjects deemed unsuitable by the investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
blood concentration of effective substance
Secondary Outcome Measures
NameTimeMethod
blood concentration of lipid parameters
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