A study to examine the postprandial levels of blood and urine parameters by test meal intake

A study to examine the postprandial levels of blood and urine parameters by test meal intake - A study to examine the postprandial levels of blood and urine parameters by test meal intake

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000055538

Enrollment

Registered

2024-09-20

Start date

2024-10-13

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 volunteers

Interventions

Intake of a test meal -&gt

Intake of a control meal Intake of a control meal -&gt

Intake of a test meal

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Males and females whose age of 20 years or more and less than 65 years 2) Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntarily participate in the study and being able to personally sign a written informed consent

Exclusion criteria

Exclusion criteria: 1) Subjects receiving a medical treatment for serious cardio-vascular, hepatic, renal, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2) Subjects whose BMI is less than 18.5 kg/m2 or 30.0 kg/m2 or more 3) Subjects drinking a lot (subjects whose pure alcohol intake per day is 60 g or more) 4) Subjects having the possibility of developing allergic symptoms by the test meal 5) Subjects whose lifestyles are irregular because of night shift or others 6) Subjects regularly taking food being rich in amino acids or proteins (supplement, beverage, etc.) 7) Subjects regularly taking medicines or quasi-drugs containing amino acids as an active ingredient 8) 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) 9) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 10) Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 11) Subjects deemed unsuitable by the investigator

Design outcomes

Primary

Measure	Time frame
analysis of 40 amino acids	—

Secondary

Measure	Time frame
blood analysis: triglycerides, glucose urinalysis: Na, K, Na/K	—

Countries

Japan

Contacts

Public ContactTomohiro Sugino

Soiken Inc. R&D Division

sugino@soiken.com06-6871-8888

Outcome results

None listed

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