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临床试验/NCT00446901
NCT00446901已完成不适用

Selenium and Prostate Cancer: Clinical Trial on Availability to Prostate Tissue and Effects on Gene Expression

Wageningen University2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2007年6月1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
入组人数
60
试验地点
2
主要终点
selenium levels in prostate tissue

研究概览

简要总结

The aim of this study is to determine whether selenium supplementation leads to changes in selenium levels and gene expression profiles in prostate tissue.

详细描述

Rationale: Prostate cancer is a frequently observed malignancy in men, especially in elderly men. Besides diagnosis and treatment, also prevention of prostate cancer is an important point of interest to reduce the incidence and mortality of prostate cancer. Selenium is considered to be a promising chemopreventive agent for prostate cancer. Exact mechanisms of chemoprevention by selenium are not fully understood. However, it is expected that selenium (among other effects) directly affects gene expression in the prostate.

Objective: The aim of this study is to get insight into bioavailability of selenium in prostate tissue and changes of gene expression profiles that might be responsible for selenium-induced chemoprevention. To meet this objective, the relationship between dietary selenium intake and changes in gene expression profiles, tissue selenium levels and blood flow in prostate tissue will be examined.

Study design: The present study is designed as a double-blind, randomized and placebo-controlled intervention trial. Blood samples, toenails, questionnaires, MR images and surgical specimens will be collected to examine effects of selenium supplementation.

Study population: The study population will consist of 60 men, diagnosed with prostate cancer and scheduled for radical prostatectomy. Written informed consent will be obtained from each participant.

Intervention: Participants will receive 300 ug selenium / day or a placebo during 5 weeks prior to radical prostatectomy. Selenium will be supplemented in the form of selenized yeast tablets (SelenoPrecise, Pharma Nord).

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

性别
Male
接受健康志愿者
否

入选标准

  • •biopsy proven prostate cancer
  • •scheduled for radical prostatectomy

排除标准

  • •liver diseases (e.g. hepatitis)
  • •kidney diseases
  • •inflammatory bowel diseases
  • •use of dietary supplements containing selenium
  • •adjuvant therapy for prostate cancer (e.g. hormonal therapy, HIFU)
  • •previously or concurrent diagnosed with cancer, other than prostate cancer

研究组 & 干预措施

Selenium (selenized yeast)

Experimental

Selenium (selenized yeast) tablets, 300 ug/day

干预措施: Selenium (Dietary Supplement)

Placebo

Placebo Comparator

Placebo

干预措施: Selenium (Dietary Supplement)

结局指标

主要结局

selenium levels in prostate tissue

时间窗: after 5 weeks of intervention with selenium or placebo

changes in gene expression profiles in prostate tissue

时间窗: after 5 weeks of intervention with selenium or placebo

次要结局

  • changes in blood flow, vessel permeability and exocrine functionality(after 5 weeks of intervention with selenium or placebo)
  • changes in gene expression profiles in blood cells(after 5 weeks of intervention with selenium or placebo)

研究者

申办方类型
Other

研究点 (2)

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