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临床试验/JPRN-UMIN000014185
JPRN-UMIN000014185已完成未知

Study of effects of food containing hop extract on reducing body fat.

Total Technological Consultant Co., Ltd. (TTC)0 个研究点目标入组 200 人开始时间: 2014年6月6日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
200

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

  • (1)(Healthy) subjects aged greater than 20 and less than 65 years old.
  • (2)Subjects with BMI greater than 25 and less than 30 kg/m^2.
  • (3)Subjects giving written informed consent.

排除标准

  • (1)Subjects who are on a diet.
  • (2)Subjects who use oral medication affecting body fat and/or lipid metabolism.
  • (3)Subjects who constantly use supplements and/or functional foods affecting body fat and/or lipid metabolism.
  • (4)Subjects who use foods containing ingredients derived from hops constantly.
  • (5)Subjects with excessive alcohol-drinking behaviors.
  • (6)Subjects who are under treatment.
  • (7)Subjects who has possibility of allergy symptoms onset.
  • (8)Subjects 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.
  • (9)Subjects who have severe anemia.
  • (10)Subjects who have a history of digestive disease affecting digestion and absorption.
  • (11)Subjects who have under treatment or a history of drug addiction and/or alcoholism.
  • (12)Subjects who are planned to become pregnant after informed consent for the current study or are pregnant or lactating.
  • (13)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire.
  • (14)Subjects who are judged as unsuitable for the study based on the results of blood test.
  • (15)Subjects who have participated in other clinical study within the last one month prior to the current study or are planned to participate in other clinical study after informed consent for the current study.
  • (16)Subjects 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.
  • (17)Subjects who are judged as unsuitable for the study by the investigator for other reason.

研究者

发起方
Total Technological Consultant Co., Ltd. (TTC)

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