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临床试验/NCT00712647
NCT00712647已完成4 期

Caret and Retinol Efficacy Trial: The Caret Coordinating Center

Fred Hutchinson Cancer Center0 个研究点目标入组 18,314 人开始时间: 2008年7月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
18,314
主要终点
Lung Cancer Incidence

研究概览

简要总结

The Carotene and Retinol Efficacy Trial (CARET) was a randomized, double-blind, placebo-controlled trial of the cancer prevention efficacy and safety of a daily combination of 30 mg of beta-carotene and 25,000 IU of retinyl palmitate in 18,314 persons at high risk for lung cancer. CARET began in 1985, and the intervention was halted in January 1996, 21 months ahead of schedule, with the twin conclusions for definitive evidence of no benefit and substantial evidence of a harmful effect of the intervention on both lung cancer incidence and total mortality. CARET continued to follow and collect endpoints on their participants through 2005. During the active intervention phase of CARET, serum, plasma, whole blood, and lung tissue specimens were collected on participants. These biospecimens make up the CARET Biorepository.

The CARET Biorepository is a valuable resource for population-based studies of the major human cancers. During CARET's twenty years of follow-up (1985-2005), we have received reports of 1,445 participants with lung cancer, 901 with prostate cancer, 433 with breast cancer, 334 with bladder cancer, 332 with colon cancer, and 1,429 with other cancers. CARET is one of the few trials that has prospectively collected serum, plasma, whole blood, blood spots (for DNA), and lung cancer tumor specimens, as well as smoking history and serial food frequency questionnaires (in some individuals for up to 12 years) in populations at high risk for lung cancer. This wealth of information in over 18,000 individuals makes the CARET Biorepository a special resource for cancer researchers.

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
45 Years 至 69 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Asbestos-exposed men who were:
  • current smokers or quit within 15 years prior to enrollment
  • had first exposure to asbestos on the job at least 15 years prior to enrollment
  • had chest X-ray positive for changes compatible with asbestos exposure according to ILO criteria; or had been employed in a protocol-defined high-risk trade for at least 5 years, at least 10 years prior to enrollment.
  • Heavy Smokers, men and women:
  • cigarette smoking history of 20+ pack-years
  • either current smokers or had quit within previous 6 years

排除标准

  • Pre-menopausal women
  • History or cirrhosis or hepatitis within 12 months prior to enrollment
  • Taking > 5500 IU daily vitamin A supplement
  • Taking any beta-carotene supplement
  • History of cancer within 5 years prior to enrollment
  • SGOT > than 2.5X upper limit of normal, or alkaline phosphatase > 1.5X upper limit of normal
  • taking less than 50% of study vitamins during the enrollment period between the First and Second Visits.

研究组 & 干预措施

1

Active Comparator

Asbestos-exposed participants and heavy smokers

干预措施: Beta Carotene and Retinol (Drug)

2

Placebo Comparator

Asbestos-exposed participants and heavy smokers

干预措施: Placebo (Other)

结局指标

主要结局

Lung Cancer Incidence

时间窗: bi-annual

次要结局

  • Other cancers(bi-annual)

研究者

申办方类型
Other

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