跳至主要内容
临床试验/JPRN-UMIN000053522
JPRN-UMIN000053522尚未招募Unknown

A study of the effect of the test food consumption on the postprandial glycemia - A study of the effect of the test food consumption on the postprandial glycemia

CPCC Company Limited0 个研究点目标入组 15 人开始时间: 2024年2月9日最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
15

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 65years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • (1) Subjects who are having Food for Specified Health Uses (FOSHU), Foods with functional claims and/or health food, including supplements, (including suppression of blood glucose level elevation, etc.) which might affect this study, three times or more a week. (2)Subjects who are taking medications (e.g., diabetes medications) that may affect this study. (3) Subjects who are participating, participated within the last four weeks before this study, or are planning to participate another clinical study of medication or health food. (4) Subjects who have extremely disheveled dietary habits. (5) Subjects who have disheveled lifestyle (e.g., shift workers and night workers). (6) Heavy drinkers (7) Subjects with abnormal thyroid function in the preliminary check. (8) Subjects who have been diagnosed as anemia or have subjective symptoms of anemia. (9) Subjects who have past and present medical history of serious diseases of heart, liver, kidney, digestive organs, and/or thyroid gland, etc. (10) Pregnant women, lactating women, or women who want to get pregnant during this study. (11) Subjects who are allergic to drugs or food. (12) Subjects who have donated over 200 mL of whole blood and/or blood components within the last one month prior to this study. (13) Male subjects who have donated over 400 mL of whole blood within the last three months prior to this study. (14) Female subjects who have donated over 400 mL of whole blood within the last four months prior to this study. (15) Male subjects whose total volume of the blood drawn within the last 12 months and this study exceed 1200 mL (16) Female subjects whose total volume of the blood drawn within the last 12 months and this study exceed 1200 mL (17) Subjects who have been determined ineligible by principal investigator or sub-investigator.

研究者

发起方
CPCC Company Limited

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