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临床试验/NCT04028739
NCT04028739已完成不适用

A Randomized, Open-label, Cross-over, Single Administration Study to Compare Bioavailability of Curcumin in Health Adults

Handok Inc.1 个研究点 分布在 1 个国家目标入组 24 人开始时间: 2019年7月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
Handok Inc.
入组人数
24
试验地点
1
主要终点
Cmax

研究概览

简要总结

A randomized, open-label, cross-over, single administration study to compare bioavailability of curcumin in health adults

详细描述

  • Randomization, Open-label, 3-period, 6-sequence, Crossover, Single
  • Drug-free inverval : more than 7 days
  • Sampling time : 0,0.5,1,1.5,2,3,4,6,8,12h

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Basic Science
盲法
None

入排标准

年龄范围
19 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Healthy adult 19 to 60 years
  • •BMI 18.0~30.0kg/m2 at screening
  • •Subject who was given, and fully understood, the information about the study, and has provided voluntary written informed consent to participate in the study and agreed to comply with the study requirements.

排除标准

  • •A person with clinically significant disease corresponding to cardiovascular, respiratory, liver, kidney, digestive system, blood/tumor system, endocrine system, immune system, neuropsychiatry or who has a history within the last 6 months.
  • •A person with a history of gastrointestinal disease or surgery (except for simple cecal surgery or hernia surgery) that may affect the absorption of food for clinical research.
  • •Persons who have an irritable reaction to foods containing turmeric or other drugs and food.
  • •Those who took medicines within 7 days before the first intake of food for clinical research.
  • •Food for Clinical Research If you have consumed foods containing turmeric (eg, radishes, curry) within 7 days before the first intake of food, or you can't consume until the day of intake of food for the last clinical study.
  • •Those who have participated in other clinical studies within 90 days prior to the first intake of food for clinical research.
  • •Women who are pregnant or lactating during screening, or who plan to become pregnant during clinical research. A person who is deemed unsuitable for participating in this clinical study because of other reasons.

研究组 & 干预措施

Theracurmin CR-033P

Experimental

1 Capsule with 150mL water, Single, curcumin 90mg/day

干预措施: curmin (Dietary Supplement)

Theracurmin CR-031P

Experimental

3 Capsule with 150mL water, Single, curcumin 90mg/day

干预措施: curmin (Dietary Supplement)

Curcumin

Experimental

1 Capsule with 150mL water, Single, curcumin 90mg/day

干预措施: curmin (Dietary Supplement)

结局指标

主要结局

Cmax

时间窗: 12hours

Maximum concentration at steady state

AUC

时间窗: 12hours

Area under the concentration-time curve at steady state

次要结局

未报告次要终点

研究者

发起方
Handok Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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