Exploratory study for intestinal environment markers.

Not Applicable

• Conditions: ot applicable

• Registration Number: JPRN-UMIN000029687
• Lead Sponsor: Suntory Global Innovation Center Ltd.

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-10-24
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up continuing
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Not provided

Exclusion Criteria

1) Subjects whose systolic blood pressure is less than 90mmHg 2) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period 3) Subjects who donated 200 mL of blood and/or blood components within four weeks prior to the current study 4) Males whose blood was collected more than 400 mL within the last three months 5) Females whose blood was collected more than 400 mL within the last four months 6) Males whose blood was collected more than 1200 mL within the last twelve months when the amount of blood sampling in the current study is added 7) Females whose blood was collected more than 800 mL within the last twelve months when the amount of blood sampling in the current study is added 8) Diabetic patients 9) Subjects who have allergic reactions to sugar alcohols 10) Subjects who are on lactose-restricted diet 11) Subjects who have any one of diseases in heart, liver, kidney or gastrointestinal tract 12) Subjects who are participating in other clinical studies for drug medicine or food, or who finished clinical study within four weeks 13) Subjects with a previous history of cardiovascular disease and digestive tract disease 14) Subjects who have allergic reaction to drug medicine 15) Subjects who drink alcohol a lot and smoke a lot 16) Subjects who have an irregular sleep cycle, work shift or work on midnight shift 17) Subjects who constantly use drug medicine affecting the test results 18) Subjects who are judged as unsuitable for the study by the principal investigator for other reasons

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Correlation between results of existing test and blood protein A levels