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临床试验/JPRN-UMIN000049370
JPRN-UMIN000049370已完成Unknown

Safety Confirmation Test by Long-term Consumption of Test Food - Safety Confirmation Test by Long-term Consumption of Test Food

Akasaka Family Clinic0 个研究点目标入组 19 人开始时间: 2022年12月16日最近更新:
适应症

试验速览

阶段
Unknown
状态
已完成
入组人数
19

研究概览

简要总结

Published at Jpn. Pharmacol. Ther. vol.51, no.6, pp.877-892 (2023)

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 64years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • Those who are currently undergoing drug treatment for some disease. Patients with a history or current history of serious disorders of the liver, kidney, heart, lungs, blood, etc. Patients with a history of co-morbidities or a history of gastrointestinal disorders. Patients with alcohol dependence or other psychiatric disorders Patients who have taken any medication for the purpose of treatment of disease in the past 1 month (except for abrupt administration of medication for headache, menstrual cramps, common cold, etc.). The specific hay fever symptoms include: Birch: alder, birch, cedar, Japanese cypress; Asteraceae: ragweed, mugwort; Poaceae: ragweed, mugwort; Poaceae: chamogaya, Japanese mugwort; and Poaceae: Japanese knotweed, Japanese millet. Persons who may develop allergic symptoms to any of the ingredients in the tested foods, or who may develop serious allergic symptoms to other foods or medicines. Persons with severe anemia Persons who have a smoking habit. Women: Pregnant, lactating, or planning to become pregnant during the study period. Those who may change their lifestyle during the study period (e.g., work at night, travel for long periods, etc.). Those who are currently, or within the past 3 months have been, or will be taking functional foods, health foods, or supplements containing the ingredients of the food under study. Those who have undergone medical treatment involving hospitalization within the past 6 months. Those who have participated in other clinical studies within one month of obtaining consent to participate in this study, or those who plan to participate in other clinical studies after obtaining consent to participate in this study. Other subjects who are judged by the investigator to be inappropriate for this study.

研究者

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