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临床试验/NCT02719860
NCT02719860已完成2 期

A Chemoprevention Trial to Study the Effects of High Tea Consumption on Smoking Related Oxidative Stress

University of Arizona0 个研究点目标入组 154 人开始时间: 2003年9月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
154
主要终点
Post-intervention change in urinary 8-hydroxydeoxyguanosine

研究概览

简要总结

The overall objective of this study is to determine the effect of high tea consumption on biological markers of oxidative stress that mediate lung cancer risk.

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
Double

入排标准

年龄范围
40 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • FEV1 < 85% and at least 25 pack-years of current or former smoking history.
  • No diagnosis of internal cancer within the last 5 years or no chemotherapy or radiation for an internal cancer within the last 5 years.
  • Meets the Southwest Oncology Group (SWOG) performance status criteria of 0-
  • Not be pregnant or intending to get pregnant during the study period (women participants).
  • Willing to drink 4 cups of tea (each cup will be brewed with 2 tea bags and 12 ounces of water) for 1-month run-in period and for the 6-month intervention period.
  • Willing to refrain from consuming other tea or tea products starting one month before the placebo run-in period and for the entire study period (a total of 8 months)
  • Willing to refrain from consuming more than one caffeinated product (coffee, soda..) starting one month before the placebo run-in period and for the entire study period (a total of 8 months).
  • Subjects cannot take mega-doses of vitamins during the trial. This is defined as more than 400 IU of vitamin E, 200 ug of selenium, or 1 gm of vitamin C per day, or more than the tolerable upper limits of any other supplement as defined in the Dietary Reference Intake panels developed by the Food and Nutrition Board under the Institute of Medicine. Such vitamin therapy must be discontinued at least 2 weeks prior to study entry.

排除标准

  • Subjects immunosuppressed by virtue of medication or disease.
  • Serious concurrent illness that could interfere with study regimen.
  • Subjects with a history of invasive cancer within the past 5 years.
  • Subjects who are drinking more than 5 cups of non-herbal tea per week.
  • Subjects who cannot or are unwilling to consume caffeinated beverages.
  • Subjects unable to perform forced expiratory maneuver during spirometry testing.
  • More than one acute emphysema exacerbation within the last 6 month -period .
  • Subjects on oxygen.
  • Women with positive urinary pregnancy test.

结局指标

主要结局

Post-intervention change in urinary 8-hydroxydeoxyguanosine

时间窗: Baseline and 6 months

Post-intervention change in urinary 8-F2-isoprostanes

时间窗: Baseline and 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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