Verification study of blood glucose level fluctuation by consumption of rice cooked in a carbohydrate-cut rice cooker -A randomized, double-blind, crossover study- - Verification study of blood glucose level fluctuation by consumption of rice cooked in a carbohydrate-cut rice cooker -A randomized, double-blind, crossover study

Others0 sites24 target enrollmentJanuary 10, 2023

ConditionsHealthy subjects

Overview

Phase: 未知
Intervention: Not specified
Conditions: Healthy subjects
Sponsor: Others
Enrollment: 24
Status: Completed
Last Updated: 2 years ago

Overview Investigators Eligibility Criteria Outcomes Similar Trials

Overview

Brief Summary

No summary available.

Registry

who.int

Start Date

January 10, 2023

End Date

March 1, 2023

Last Updated

2 years ago

Study Type

Interventional

Sex

All

Investigators

Sponsor

Others

Eligibility Criteria

Inclusion Criteria

Not provided

Exclusion Criteria

•1\. Subjects who have been diagnosed with diabetes by a physician. 2\. Subjects who are currently receiving medication or outpatient treatment for some serious disease. 3\. Subjects who are currently undergoing exercise or diet therapy under the supervision of a physician. 4\. Subjects who may develop allergies to the test food. 5\. Subjects who have a current or a history of drug dependence or alcohol dependence. 6\. Subjects who are hospitalized for mental disorders (depression, etc.) or sleep disorders(insomnia, sleep apnea, etc.), or have a history of mental disorders in the past. 7\. Subjects who are with extremely irregular eating, sleeping, or other habits. 8\. Subjects who have an extremely unbalanced diet. 9\. Subjects who have or have had serious diseases such as brain diseases, malignant tumors, immune diseases, diabetes, liver diseases (hepatitis), kidney diseases, heart diseases, etc., thyroid diseases, adrenal diseases, and other metabolic diseases. 10\. Subject who use health foods and medicines that contain ingredients that affect blood glucose levels. 11\. Subjects who have participated in other clinical trials (research) within 3 months retrospectively from the date of obtaining consent, or those who have plans to participate in other clinical trials (research) during the study period 12\. Subjects who have collected more than 200 mL of blood within 1 month or 400 mL within 3 months prior to the date of obtaining consent. 13\. Subjects who are currently pregnant or breastfeeding. or who are likely to become so during the study period. 14\. Subjects who have difficulty in complying with the recording of various questionnaires. 15\. Subjects who are judged to be inappropriate as subjects based on clinical laboratory test values and measured values at the time of SCR. 16\. Other subjects who are judged unsuitable as subjects by the principal investigator.