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Study to confirm the effect of single ingestion of the test food on Na excretion in the urine

Not Applicable
Conditions
Healthy adults
Registration Number
JPRN-UMIN000049458
Lead Sponsor
Social Medical Care Corporation Taiseikai Fukuoka Kinen PET Kenshin Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who have a serious medical history and a history of gastrointestinal resection surgery (excluding appendectomy and endoscopic polypectomy) (2) Subjects who have a current history of internal disease , including, in particular, failure of kidney function and voiding of urine (3) Subjects who have allergies to any ingredients in the test food or the unified meals (4) Heavy alcohol drinkers (>60g of pure alcohol/day) or excessive smokers (>20 cigarettes/day) who cannot quit smoking during the study under the unified management (5) Subjects who wish to become pregnant during the study, pregnant women (including those who may be pregnant) or breastfeeding (6) Subjects who are participating in a study to take other test foods or drugs, or a study to apply cosmetics or drugs, or those who plan to participate other study during this study (7) Subjects who may need to avoid ingesting ingredients whose origin is not clearly indicated in the food and drink used in the study due to religious reasons, etc. (8) Late night workers, those who frequently work long overtime or work irregular shifts. (9) Subjects who did not test negative for SARS-Cov-2 in the secondary screening (10) Subjects who take food containing the test food every day (11) Subjects who habitually consume health foods, quasi-drugs, and pharmaceuticals that have a hypotensive effect (12) Subjects whose evaluable data cannot or could not be obtained due to menstruation on a test day (13)Subjects who are judged to be inappropriate for this study by the principal investigator with other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total amount of Na excreted in the urine in 24 hours
Secondary Outcome Measures
NameTimeMethod
Total urine volume, Na concentration of the urine collected in each time frame, Na amount of the urine collected in each time frame, Body water in each site measured with body composition analyzer
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