跳至主要内容
临床试验/JPRN-UMIN000051056
JPRN-UMIN000051056已完成Unknown

Test Study on the effect of food intake on postprandial blood glucose level - Test Study on the effect of food intake on postprandial blood glucose level

others0 个研究点目标入组 10 人开始时间: 2023年5月16日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 60years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Subjects who have or have had diabetic diseases. 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 history of drug dependence or alcohol dependence. 6.Subjects who are hospitalized for mental disorders (depression, etc.) or sleep disorders, or have a history of mental disorders in the past. 7.Subjects who have irregular rhythm of life due to night work or shift work. 8.Subjects who are with extremely irregular eating, sleeping, or other habits. 9.Subjects who have an extremely unbalanced diet. 10.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. 11.Subjects whose fasted blood glucose levels are 126 mg/dL or more or HbA1c levels are 6.5% or more. 12.Subject who use health foods and medicines that contain ingredients that affect blood glucose levels. 13.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. 14.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. 15.Subjects who are currently pregnant or breastfeeding. or who are likely to become so during the study period. 16.Subjects who have difficulty in complying with the recording of various questionnaires. 17.Subjects who are judged to be inappropriate as subjects based on clinical laboratory test values and measured values at the time of SCR.

研究者

发起方
others

相似试验