Clinical Trials Directory

Trials / Completed

CompletedNCT00064194

Vitamin E, Selenium, and Soy Protein in Preventing Cancer in Patients With High-Grade Prostate Neoplasia

A Double-Blind, Placebo-Controlled, Randomized Study Of Combination Vitamin E, Selenium And Soy Protein Product In Subjects With High Grade Prostatic Intraepithelial Neoplasia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
310 (actual)
Sponsor
NCIC Clinical Trials Group · Network
Sex
Male
Age
120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Chemoprevention therapy is the use of certain substances to try to prevent the development or recurrence of cancer. Vitamin E, selenium, and soy protein may be effective in preventing the development of prostate cancer. PURPOSE: Randomized phase III trial to study the effectiveness of combining vitamin E, selenium, and soy protein in preventing prostate cancer in patients who have high-grade prostate neoplasia.

Detailed description

OBJECTIVES: * Determine whether nutritional supplementation with soy protein isolate, vitamin E, and selenium can delay the time to development of invasive prostate cancer (disease-free survival) in patients with high-grade prostatic intraepithelial neoplasia. * Determine the effect of this supplementation on intermediate endpoints that may reflect a lessened risk of invasive prostate cancer (e.g., serum PSA levels, hormone levels, lycopene, malondialdehyde, vitamin E, and reduced thiol groups) in these patients. * Determine the safety of this supplementation in these patients. OUTLINE: This is a randomized, double-blind, multicenter study. Patients are stratified according to participating center. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients receive oral vitamin E, oral selenium, and oral soy protein isolate twice daily. * Arm II: Patients receive oral placebo twice daily. In both arms, treatment continues for 3 years in the absence of invasive prostate cancer (demonstrated on biopsy) or unacceptable toxicity. Patients are followed every 3 months for 1 year and then every 6 months for 2 years. PROJECTED ACCRUAL: A total of 306 patients (153 per treatment arm) will be accrued for this study within 6 years.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTselenium
DIETARY_SUPPLEMENTsoy protein isolate
DIETARY_SUPPLEMENTvitamin E

Timeline

Start date
2001-11-28
Primary completion
2008-04-30
Completion
2008-04-30
First posted
2003-07-09
Last updated
2020-04-03

Locations

3 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00064194. Inclusion in this directory is not an endorsement.