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临床试验/NCT01008020
NCT01008020已完成不适用

A Randomized Controlled Study on the Effects of Tea Catechin Consumption on the Prevention of Influenza Infection in Healthy Adults

Masahiro Morikawa2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2009年11月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
200
试验地点
2
主要终点
the incidence rates of influenza infection

研究概览

简要总结

The Purpose of this study is to evaluate the effects of 5 months catechin consumption on the prevention of influenza infection.

详细描述

Catechins are the major components of tea flavonoids and are reported to possess physiological activities such as antiviral effects. Recent experimental studies have revealed that tea catechin extracts prevent influenza infection, but few studies have been conducted on the clinical effects of tea catechin consumption on the prophylaxis of influenza infection. Based on these backgrounds, we designed a prospective randomized controlled study to evaluate the effects of 5 months tea catechin consumption on the prophylaxis of influenza infection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • aged over 20 years
  • possible to maintain without drinking tea more than 250 ml per day during the study
  • possible to maintain without taking supplements or herbal products including catechin extracts during the study
  • possible to fill out a questionnaire personally
  • Obtained written informed consent before participation

排除标准

  • Possessing some chronic infectious diseases in need of therapy
  • Possessing tea or catechin allergy
  • Possessing a history of influenza infection before six months prior to the study
  • diagnosed as inadequate for other reasons to participate the study by principal investigator

结局指标

主要结局

the incidence rates of influenza infection

时间窗: Until 5 months consumption of the study capsules

次要结局

  • the incidence rates of upper respiratory tract infections(Until 5 months consumption of the study capsules)
  • the severity of the symptoms and the duration of the cold among incident cases(Until 5 months consumption of the study capsules)
  • occurrence of the adverse events(Until 5 months consumption of the study capsules)

研究者

发起方
Masahiro Morikawa
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Masahiro Morikawa

Clinical Trials management office

University of Shizuoka

研究点 (2)

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