Breast Cancer Clinical Trial

Soy Isoflavones and Breast Cancer Risk Reduction

Summary

Soy consumption has been associated with reduced risk for developing breast cancer. Soy contains isoflavones which are weak estrogens. The roles of soy isoflavones in reducing breast cancer risk are currently unclear. Breast density has been considered as a breast cancer risk marker. We hypothesize that because isoflavones have estrogen-like activities, breast density and possibly bone density will be lower in women on soy-isoflavones.

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Full Description

This is a randomized, double-blind study, with two arms and 100 women in each arm. Premenopausal women will be recruited and randomly allocated to take one of the two different dietary supplements in pills daily for 2 years. The two supplements are soy isoflavones (treatment) and placebo (carbohydrates). Both treatment and placebo pills will contain multi-vitamins and minerals. Multiple blood, urine, and breast fluid samples will be obtained before and during the dietary supplement periods and analyzed for biomarkers of breast cancer risk. At baseline and after the intervention period, breast density and bone density will be assessed by radiologic techniques. The efficacy of the dietary intervention will be determined by comparing mean changes of serum markers for breast cancer risk,dense breast tissue, and bone mineral density over the two year dietary intervention period in the two supplement groups with adjustment for baseline values and individual patient characteristics of interest. We predict that 2 years of soy isoflavone supplement will reduce breast density, which may be explained by individual changes in serum markers of breast cancer risk.

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Eligibility Criteria

Inclusion Criteria:

healthy premenopausal women
30 to 42 years old
normal mammograms
regular menstrual cycles

Exclusion Criteria:

abnormal mammograms
first degree relatives with breast cancer
pregnant or lactating
peri- or post-menopause
breast augmentation, reduction or lifting
on oral contraceptive medications or exogenous hormones
medically prescribed diets
allergic reaction to soy products

Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

197

Study ID:

NCT00204490

Recruitment Status:

Active, not recruiting

Sponsor:

The University of Texas Medical Branch, Galveston

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There is 1 Location for this study

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General Clinical Reserach Center, The University of Texas Medical Branch
Galveston Texas, 77555, United States

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Study is for people with:

Breast Cancer

Phase:

Phase 2

Estimated Enrollment:

197

Study ID:

NCT00204490

Recruitment Status:

Active, not recruiting

Sponsor:


The University of Texas Medical Branch, Galveston

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