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The Specific Role of Isoflavones in Reducing Prostate Cancer Risk

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Prevastein HC®
Placebo
Sponsored by
H. Lee Moffitt Cancer Center and Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prostate Cancer focused on measuring isoflavones, soy

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Males, between the ages of 50 and 80
  • Diagnosed with grade 1-2 prostate cancer (Gleason Score 2 to 6) Note: patients with a Gleason primary pattern 4 (4+1 or 4+2) are not eligible.
  • No prior or current therapy for prostate cancer
  • No other history of cancer except non-melanoma skin cancer
  • No known history of hepatic and/or renal disease
  • No evidence of prostatitis or urinary tract infection (men being treated with antibiotics may be enrolled 30 days after completion of therapy given that they still meet all other eligibility criteria)
  • No antibiotic use within 30 days of registration
  • Close to ideal body weight(Body Mass Index no greater than 32 Kg/m²)
  • Omnivorous diet
  • Able and willing to give written consent

Exclusion Criteria:

  • Less than 50 years or over 80 years of age
  • Prostate cancer beyond grade 2 (Gleason Score greater than 6)
  • Gleason primary pattern 4 (4+1 or 4+2)
  • Prior or planned treatment for prostate cancer of any stage
  • Prior history of other cancer except non-melanoma skin cancer
  • Current use of nutritional supplements, including modular supplements of other agents with antioxidant properties e.g. retinoids, beta-carotene, and isoflavones
  • Allergy to study agent
  • Known history of hepatic or renal disease
  • Body Mass Index greater than 32 Kg/m²
  • Vegetarian/vegan diet
  • Diet high in soy products (men who routinely consume a diet high in soy products may be enrolled 30 days after eliminating soy product from the diet)
  • Prostatitis or urinary tract infection
  • Treatment with antibiotics within 30 days of registration

Sites / Locations

  • H. Lee Moffitt Cancer Center and Research Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

A

B

Arm Description

Dietary Supplement: Prevastein HC®

Placebo

Outcomes

Primary Outcome Measures

Observe the effects of the 12 - week intervention with isoflavones on sex hormones and PSA, a marker of disease progression.

Secondary Outcome Measures

Full Information

First Posted
February 5, 2008
Last Updated
September 21, 2012
Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Cognis
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1. Study Identification

Unique Protocol Identification Number
NCT00617617
Brief Title
The Specific Role of Isoflavones in Reducing Prostate Cancer Risk
Official Title
The Specific Role of Isoflavones in Reducing Prostate Cancer Risk
Study Type
Interventional

2. Study Status

Record Verification Date
February 2010
Overall Recruitment Status
Completed
Study Start Date
February 2002 (undefined)
Primary Completion Date
May 2007 (Actual)
Study Completion Date
May 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
H. Lee Moffitt Cancer Center and Research Institute
Collaborators
Cognis

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to determine if giving men with early stage (Grade 1-2) prostate cancer dietary supplement from soybeans called isoflavones, will change their blood hormone levels. Isoflavones are substances found in a high concentration in soybeans that are converted in the intestines to hormone-like compounds which are similar to estrogen. They are also thought to have cancer fighting properties. Clinical trials suggest that isoflavones can increase certain sex hormones, which results in the slower production of prostate cancer cells. This study will determine if adding isoflavones (supplied as Prevastein HC®) 80 mg/day in a pill form can change your risk factors that cause early stage prostate cancer to progress to more advanced disease.
Detailed Description
To prevent biasing the outcome of the study, this is a double-blind study design, where both the trialists and the participants are blinded to the specific nature of the product (isoflavones and placebo). Participants in both groups will be discouraged from increasing their intake of dietary isoflavones in the form of tofu, soy beans, soy milk, etc. In addition, the intervention does not include active counseling on dietary modification and supplementation of any one group. Monthly appointments will be made for all participants for data collection and toxicity assessment. Schema: This is a controlled, randomized, double blinded clinical trial, having one experimental and one control group (n - 75/arm). Participants in the experimental group will consume an isoflavones supplement in the form of Prevastein HC®, which will deliver 80 mgs (40 mg/dose) biologically active isoflavones and those in the control group will receive an identical placebo. The isoflavones supplement and the placebo tablets will be manufactured and packaged by Cognis Corporation. Isoflavones will be supplied at no charge by Cognis Corporation, LaGrange, Illinois as Prevastein HC®. Each Prevastein HC® tablet delivers 20 mg biologically active isoflavones, which is available for absorption. Participants will consume 2 tablets twice daily (with meals) in addition to their usual diet. Placebo will be supplied at no charge by Cognis Corporation, LaGrange, Illinois as an indistinguishable tablet. Participants will consume 2 tablets twice daily (with meals) in addition to their usual diet. A standardized multivitamin will be supplied at no charge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
isoflavones, soy

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Dietary Supplement: Prevastein HC®
Arm Title
B
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Prevastein HC®
Intervention Description
Experimental Group - Participants in the experimental group will consume an isoflavones supplement in the form of Prevastein HC®, which will deliver 80 mgs (40 mg/dose) biologically active isoflavones.
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Control Group - Control Group participants will receive an identical placebo.
Primary Outcome Measure Information:
Title
Observe the effects of the 12 - week intervention with isoflavones on sex hormones and PSA, a marker of disease progression.
Time Frame
12 week treatments

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males, between the ages of 50 and 80 Diagnosed with grade 1-2 prostate cancer (Gleason Score 2 to 6) Note: patients with a Gleason primary pattern 4 (4+1 or 4+2) are not eligible. No prior or current therapy for prostate cancer No other history of cancer except non-melanoma skin cancer No known history of hepatic and/or renal disease No evidence of prostatitis or urinary tract infection (men being treated with antibiotics may be enrolled 30 days after completion of therapy given that they still meet all other eligibility criteria) No antibiotic use within 30 days of registration Close to ideal body weight(Body Mass Index no greater than 32 Kg/m²) Omnivorous diet Able and willing to give written consent Exclusion Criteria: Less than 50 years or over 80 years of age Prostate cancer beyond grade 2 (Gleason Score greater than 6) Gleason primary pattern 4 (4+1 or 4+2) Prior or planned treatment for prostate cancer of any stage Prior history of other cancer except non-melanoma skin cancer Current use of nutritional supplements, including modular supplements of other agents with antioxidant properties e.g. retinoids, beta-carotene, and isoflavones Allergy to study agent Known history of hepatic or renal disease Body Mass Index greater than 32 Kg/m² Vegetarian/vegan diet Diet high in soy products (men who routinely consume a diet high in soy products may be enrolled 30 days after eliminating soy product from the diet) Prostatitis or urinary tract infection Treatment with antibiotics within 30 days of registration
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nagi B. Kumar, PhD., RD
Organizational Affiliation
H. Lee Moffitt Cancer Center and Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
H. Lee Moffitt Cancer Center and Research Institute
City
Tampa
State/Province
Florida
ZIP/Postal Code
33612
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Specific Role of Isoflavones in Reducing Prostate Cancer Risk

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