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Clinical Trials/JPRN-UMIN000021481
JPRN-UMIN000021481
Completed
未知

Study of effect of food containing plant ingredient on postprandial serum uric acid - Study of food containing plant ingredient on postprandial serum uric acid

TTC Corporation0 sites20 target enrollmentApril 29, 2017

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
TTC Corporation
Enrollment
20
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 29, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
TTC Corporation

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\)Individuals who use oral medication or supplements or functional foods affecting uric acid metabolism. (2\)Individuals who is not suitable for subjects by pre\-test questionnaire. (3\)Individuals who declare the allergy symptoms against test diets. (4\)Individuals who have a chronic disease and use medicines continuously. (5\)Individuals who have a history of serious disease (e.g., diabetes, liver disease, kidney disease, and/or heart disease), thyroid gland disease, adrenal gland disease, and/or metabolic disorder. (6\)Individuals who have a history of digestive disease affecting digestion and absorption. (7\)Individuals who are judged as unsuitable for the study based on the results of blood test. (8\)Individuals who are planned to participate in other clinical study. (9\)Individuals who have donated over 200 mL of blood and/or blood component within the last one month prior to the current study or over 400 mL of blood and/or blood component within the last three months prior to the current study. (10\)Individuals with excessive alcohol\-drinking behaviors (over 20 g alcohol/day). (11\)Individuals who can't stop drinking for 3 days until the pre\-check day and check days. (12\)Individuals who is diagnosed as severe anemia and not suitable for frequent collection of blood. (13\)Individuals who have under treatment or a history of drug addiction and/or alcoholism. (14\)Individuals who are planned to become pregnant after informed consent for the current study or are pregnant or lactating. (15\)Individuals who are working for a functional food company. (16\)Individuals who are judged as unsuitable for the study by the investigator for other reason.

Outcomes

Primary Outcomes

Not specified

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