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NCT Number: NCT00446901

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

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

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Key information

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

University Medical Centre St Radboud, Nijmegen, Gelderland, Netherlands

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About this study

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).

Main study parameters: Levels of selenium in prostate tissue and changes in prostate gene expression profiles of participants supplemented with selenium or placebo, compared before and after the short intervention period, will be considered as the main parameters of the present study. Besides gene expression profiles in prostate tissue, also gene expression profiles of peripheral mononuclear cells (PBMC), levels of selenium in blood and toenails and blood flow and permeability of blood vessels of prostate tissue will be analyzed.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • 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

Treatment and study plan

Selenium

Dietary Supplement

Selenized yeast, 300 ug/day

Other names: SelenoPrecise, PharmaNord

Primary outcomes

  1. selenium levels in prostate tissue

    Time frame: after 5 weeks of intervention with selenium or placebo

  2. changes in gene expression profiles in prostate tissue

    Time frame: after 5 weeks of intervention with selenium or placebo

Secondary outcomes

  1. changes in blood flow, vessel permeability and exocrine functionality

    Time frame: after 5 weeks of intervention with selenium or placebo

  2. changes in gene expression profiles in blood cells

    Time frame: after 5 weeks of intervention with selenium or placebo

Sponsors and collaborators

Lead sponsor

Wageningen University

Other

Collaborators

  • World Cancer Research Fund International

Registry information

Acronym: SePros

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
Mar 13, 2007
Registry last updated
Mar 14, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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