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CompletedNCT00200824Updated Mar 12, 2009

Effects of Soy Compounds on Breast Cancer, Prostate Cancer, and Bone Health

A Phase 2 interventional study of Soy Isoflavone Nutritional Supplements in Breast Cancer and Prostate Cancer, sponsored by National Center for Complementary and Integrative Health (NCCIH). Completed at 1 site in United States. Per ClinicalTrials.gov, last updated 2009-03-12.

Sponsored by National Center for Complementary and Integrative Health (NCCIH) · Phase 2, Interventional, and Prevention

Phase
Phase 2
Study type
Interventional
Allocation
Randomized
Sex
All
01

Study summary

This study will determine the effects of soy products on in vitro surrogate cancer markers as well as bone density markers and quality of life parameters in men and women. This study will also determine concentrations of isoflavones (naturally occurring plant compounds that act like estrogen in the body) in prostate tissue that has been removed during prostatectomy, as well as in the blood.

Read the detailed description

In the United States, consumption of soy products has dramatically increased in the past several years. Foods made from soy are high in isoflavones and evidence suggests that these isoflavones, genistein in particular, have many beneficial properties such as alleviating menopausal side effects and reducing the risk of osteoporosis, breast cancer, and prostate cancer. However, this data has been derived largely from studies with animal or cell models; human trials are limited. This study will determine the effects of soy isoflavones on quality of life and cancer and bone density markers.

While isoflavones have been purported to inhibit the proliferation of cancer cells, the concentrations required for this anti-cancer effect were determined to be much higher than the concentrations that can be achieved in plasma after intake of isoflavones. Recent animal studies have suggested that isoflavones may be concentrated 10-fold in tissue compared to blood concentrations. If this is true, then the higher concentration would be in the range found in the cancer cell line research to be protective of cancer. This study will determine whether tissue concentrations are similar to, higher than, or different than blood concentrations.

This study will last 5 years and will comprise three populations: men with prostate cancer on androgen ablation therapy, postmenopausal women on hormone replacement therapy (HRT), and postmenopausal women not on HRT. Participants will be randomly assigned to receive either isoflavone or placebo for two to four weeks. Participants' serum and serum extracts will be incubated with cultured human cell lines (prostate cancer, breast cancer and osteoblasts) and estrogenic and non-estrogenic mechanisms of action investigated. The human sera data will be complemented by parallel studies of direct addition of crystalline isoflavones (genistein, daidzein and equol) to the same cultured human cell lines. Participant's serum and urine also will be tested for markers of bone resorption and formation. Quality of life issues will be assessed with questionnaires.

02

Conditions studied

  • Breast Cancer
  • Prostate Cancer

Keywords

  • isoflavones
  • soy
  • postmenopausal
  • men
  • prostate
  • breast
  • bone
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

Browse Breast Neoplasms studies →

Lead sponsor

National Center for Complementary and Integrative Health (NCCIH) is the lead sponsor of 218 studies on the registry; 7 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Scheduled for prostatectomy
  • Willing and able to consume study tablets for at least 2 weeks prior to surgery
  • Willing to accept random assignment
  • Signed informed consent

Exclusion criteria

Exclusion Criteria

  • Unwilling to avoid soy intake during the study period
  • Currently taking antibiotics
05

Study design

Phase
Phase 2
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double

Interventions

  • DrugSoy Isoflavone Nutritional Supplements
06

What researchers measure

Primary outcomes

  1. Markers of Bone Density

  2. Basic Science (e.g., proliferation of cancer cells in vitro)

Secondary outcomes

  1. Bioavailability

07

Study locations

1 site
  • Christopher Gardner
    Stanford, California 94305-5705, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2009, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00200824
Lead sponsor
National Center for Complementary and Integrative Health (NCCIH)
First posted
Sep 20, 2005
Start date
May 2000
Completion
Jan 2005
Last update
Mar 12, 2009

Study contacts

Christopher Gardner
principal investigator · Stanford University
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2006. You cannot join it, but the record below documents what was studied.

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