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Examination of postprandial urinary salt excretion during test food intake for adult males

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000042221
Lead Sponsor
TTC Co., Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
16
Inclusion Criteria

Not provided

Exclusion Criteria

(1) Subjects who are going to the hospital or taking medication for the treatment of dysuria (2) Subjects who are on or will be on a diet during the study period (3) Subjects with excessive drinking habits (4) Subjects who habitually take health foods, quasi-drugs, and medicines that have a blood pressure lowering effect (5) Subjects with smoking habits (6) Subjects currently diagnosed with arrhythmia (7) Subjects who take health foods, quasi-drugs, and medicines that strengthen the ingredients involved in research foods at least once a week (8) Subjects who take health foods, quasi-drugs, and medicines that are said to be effective in salt excretion at least once a week (9) Subjects with or with renal disease, urethral stones (10) Subjects having a disease requiring treatment or a history of serious diseases for which medication was required (11) Subjects having a disease requiring treatment or a history of serious diseases for which medication was required (12) Subjects having possibilities for emerging allergy related to the study (13) Subjects whose physical measurements and physical examination values before the start of ingestion were significantly out of the standard range (14) 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 (15) Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (16) Subjects judged as unsuitable for the study by the investigator for other reasons

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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