Effect of a Natural Health Product on Urinary Estrogen Metabolites

Nutrasource

Status and phase

Completed

Phase 2

Phase 1

Conditions

Breast Cancer

Treatments

Dietary Supplement: FemMED Breast Health Formula

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT01089049

NHPD136987 (Other Identifier)

NDI: 136987

Details and patient eligibility

About

The purpose of this study is to determine if a supplemental formula can beneficially alter the ratio of urinary estrogen metabolites.

Full description

The active botanical constituents in femMED Breast Health Formula contain lignans, compounds with anti-estrogenic activity, that have been shown to exert an estrogenic effect during the follicular phase [i.e. when estrogen is low] and an antiestrogenic effect in the luteal phase of a female menstrual cycle. These are plant-derived chemicals that can act as weak mimics of estrogen in the body. Overall these compounds have been found to be helpful in stabilizing the natural cyclical fluctuation of estrogen levels.

The trial will be a double-blind, placebo-controlled parallel study in which 100 subjects will be recruited to one of two arms of the study: one arm will consist of pre-menopausal women; another will consist of post-menopausal women. Each arm of the study will be carried out concurrently and in one phase, with no washout period. The placebo assignment will be randomized within each arm of the study.

Subjects in each arm of the study will follow the same protocol. Urine and blood samples will be collected from each group at both the first and last visit, and subjects will receive a month's supply of treatment or placebo at the first visit, which they will consume on a daily basis until their second lab visit 28 days later. Urine samples will be analyzed for the following estrogen metabolites: 2-OH-estrone and 16-α OH-estrone. Blood samples would be collected and assessed for levels of enterolactone. Pre and post-supplementation results will be assesses for any differences by statistical comparison.

Enrollment

98 patients

Sex

Female

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

18 years of age or older
Healthy
Willing to collect urine samples and to have blood drawn
Post-menopausal and have not taken hormone replacement therapy (HRT) in the past year (48 subjects)
Pre-menopausal (48 subjects)

Exclusion criteria

Diagnosed with any major illness(e.g. cancer)
Diabetes, thyroid disease, atypical hyperplasia, fibrocystic breast disease, family history of ovarian cancer, a history of "migraines with aura"
Women taking blood thinner or thyroid medication (including warfarin)
Known allergy to any of the any of the study ingredients
Pregnancy or lactation
Regular consumption in the previous 3 months of any other natural health products (NHPs) or pharmaceutical containing ingredients with a similar effect on estrogen metabolism as those included in the femMED Breast Health treatment
Family history of breast cancer risk
Post-menopausal women on HRT
Pre-menopausal women taking hormonal contraceptives (oral contraceptives, the patch etc.)
All other forms of estrogen, progesterone and/or androgens (i.e. testosterone therapy)