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临床试验/NCT00063453
NCT00063453已完成3 期

The Respiratory Ancillary Study (RAS) to SELECT

Cornell University0 个研究点目标入组 2,920 人开始时间: 2003年8月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
2,920
主要终点
Change in pulmonary function over time by arm of study

研究概览

简要总结

To test whether supplementation with selenium and/or vitamin E affects pulmonary function.

详细描述

BACKGROUND:

There is compelling evidence from observational epidemiologic studies that intakes of nutrients with antioxidant properties are associated with reduced risks of chronic obstructive disease (COPD) and increased lung function. This study is ancillary to the multisite Selenium and Vitamin E Cancer Prevention Trial (SELECT), a 4-arm placebo-controlled, double-blinded randomized trial in 35,000 men testing whether daily supplementation with vitamin E (400mg alpha-tocopherol), selenium (200 micrograms selenomethionine) or both vitamin E and selenium can prevent prostate cancer.

DESIGN NARRATIVE:

This study is ancillary to the multisite Selenium and Vitamin E Cancer Prevention Trial (SELECT), a 4-arm placebo-controlled, double-blinded randomized trial in 35,000 men testing whether daily supplementation with vitamin E (400mg alpha-tocopherol), selenium (200 micrograms selenomethionine) or both vitamin E and selenium can prevent prostate cancer. A total of 3,000 SELECT participants will be enrolled for this respiratory ancillary study, and data collection will be extended to include pulmonary function, respiratory disease, and respiratory symptoms. Biological measures of nutrient exposure (serum vitamin E and selenium) and plasma lipids (total and high-density lipoprotein cholesterol) will be collected on all participants and oxidant burden (urinary F2-isoprostane) on a sub sample of heavy smokers and men with COPD. The primary outcome will be change over about 36 months in forced expiratory volume in the first second (FEV1). FEV1 is a valid and reliable measure of respiratory function that strongly predicts COPD and mortality. Extensive data on diet and dietary supplement use are being collected by the SELECT parent study. All specific aims examine pre-specified contrasts between the 4 arms of the SELECT randomized trial. The underlying hypothesis is that supplements will reduce the age related decline in FEV1 and thus at the 3-year follow-up FEV1, which will be tested in longitudinal and cross-sectional models. A secondary aim considers whether the effect of supplementation is greater among smokers (high burden of exogenous oxidants) who, by purposive selection of the study sites, will comprise about 25% of the sample.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Factorial
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者
是

入选标准

  • •Eligibility criteria:
  • •age ≥ 55 y (≥ 50 y in African-Americans)
  • •serum prostate-specific antigen ≤ 4ng/mL
  • •no clinical evidence of prostate cancer

排除标准

  • •Off both SELECT supplements

研究组 & 干预措施

Vitamin E and selenium

Experimental

Vitamin E and selenium combined

干预措施: Selenium (Dietary Supplement)

Selenium and vitamin E placebo

Experimental

Selenium alone

干预措施: Vitamin E placebo (Dietary Supplement)

vitamin E Placebo and Selenium placebo

Placebo Comparator

Double placebo

干预措施: Vitamin E placebo (Dietary Supplement)

vitamin E Placebo and Selenium placebo

Placebo Comparator

Double placebo

干预措施: Selenium placebo (Dietary Supplement)

Vitamin E and selenium

Experimental

Vitamin E and selenium combined

干预措施: Vitamin E (Dietary Supplement)

Selenium and vitamin E placebo

Experimental

Selenium alone

干预措施: Selenium (Dietary Supplement)

Vitamin E and selenium placebo

Experimental

Vitamin E alone

干预措施: Selenium placebo (Dietary Supplement)

Vitamin E and selenium placebo

Experimental

Vitamin E alone

干预措施: Vitamin E (Dietary Supplement)

结局指标

主要结局

Change in pulmonary function over time by arm of study

时间窗: Outcome is assessed at annual and bi-annual study visits, during in-person visit of participant to the study site. Over a period of about 36 to 48 months, participants are assessed between 3 and 4 times

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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