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Completed

NCT Number: NCT00626769

Third Year Evaluation on Genistein Efficacy and Safety

BACKGROUND: Recent evidences showed that the phytoestrogen genistein positively affects bone metabolism with no clinically significant adverse effects in a cohort of osteopenic, postmenopausal women. However, there is still a knowledge gap regarding the long-term safety of genistein on the breast, the uterus, the thyroid gland and its efficacy in postmenopausal women.

OBJECTIVE: To assess the safety profile of genistein on mammary and thyroid glands and endometrium and cardiovascular apparatus and its effects on bone metabolism after a 3-year therapy with pure, standardized genistein (54 mg/day).

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Key information

Age range

49 year–67 year

Sex eligibility

Female

Study type

Observational

About this study

DESIGN: The parent study was a randomized, double-blind, placebo-controlled trial involving 389 osteopenic, postmenopausal women for 24 months. After the 24-month visit, a sub-population (138 patients) accepted to continue the intervention until 36 months, thus generating a follow-up study.

SETTING: 3 Italian university medical centers. INTERVENTIONS: Participants received 54 mg of genistein, daily, (n=71) or placebo (n=67). Both intervention and placebo contained calcium and vitamin D3. All patients also received dietary instruction in an isocaloric fat-reduced diet.

MEASUREMENTS: Mammographic breast density at baseline and after 24 and 36 months was assessed by visual classification scale and by digitized quantification. BRCA1 and BRCA2 molecular message, sister chromatid exchanges and endometrial thickness were also evaluated at the same time points. Measurements of lumbar spine and femoral neck BMD and QUS t-score were assayed in our patients. Secondary outcomes were serum levels of B-ALP, IGF-I, sRANKL, osteoprotegerin and urinary excretion of CTX, pyridinoline and deoxypyridinoline. Furthermore insulin resistance (HOMA-IR), glucose levels, homocysteine and hot flushes were also evaluated. In addition for thyroid safety TSH, fT3, fT4, thyroid autoantibodies, and mRNA for thyroid and retinoid receptors were evaluated.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Good general health
  • Have not had a menstrual period in the preceding year
  • Had not undergone surgically induced menopause
  • Had a follicle-stimulating hormone level > 50 IU/liter and a serum 17 beta-estradiol level ≤ 100 pmol/liter
  • Established osteopenia (-1<T-score<-2.5 SD)

Exclusion criteria

  • Clinical or laboratory evidence of confounding systemic diseases, such as cardiovascular, hepatic, or renal disorders
  • Coagulopathy, use of oral or transdermal estrogen, progestin, androgen or other steroids
  • Biphosphonates, cholesterol-lowering therapy or cardiovascular medications in the preceding six months
  • Smoking habit of more than two cigarettes per day
  • Previous treatment with any drug that could affect the skeleton in the preceding year
  • A family history of estrogen-dependent cancer
  • BMD at femoral neck > 0.795 g/cm2; this BMD value corresponds to a T score of -1 standard deviation

Treatment and study plan

aglycone genistein

Dietary Supplement

2 capsules per day containing 27 mg of aglycone genistein, calcium carbonate (500 mg) and vitamin D (400 IU), for a 3-year period.

Other names: Genivis, Fosteum

Placebo

Dietary Supplement

2 capsules per day containing calcium carbonate (500 mg) and vitamin D (400 IU), for a 3-year period.

Primary outcomes

  1. Bone Mineral Density

    Time frame: basal and after 1 year

  2. Mammographic breast density

    Time frame: basal and after 3 years

Secondary outcomes

  1. Bone-specific alkaline phosphatase (B-ALP)

    Time frame: basal and after 1 year

  2. Insulin-like growth factor 1 (IGF-1)

    Time frame: basal and after 1 year

  3. Pyridinium cross-links (pyridinoline and deoxypyridinoline)

    Time frame: basal and after 1 year

  4. carboxy-terminal cross-linking telopeptide (CTX)

    Time frame: basal and after 1 year

  5. Osteoprotegerin and soluble receptor activator of NF-kB ligand (s-RANKL)

    Time frame: basal and after 1 year

  6. BRCA1 and BRCA2 mRNA levels

    Time frame: basal and after 3 years

  7. Sister Chromatid exchanges

    Time frame: basal and after 3 years

  8. Endometrial thickness

    Time frame: basal and after 3 years

  9. Insulin resistance

    Time frame: basal and after 3 years

  10. hot flushes

    Time frame: basal and after 3 years

  11. Thyroid status

    Time frame: basal and after 3 years

Sponsors and collaborators

Lead sponsor

University of Messina

Other

Collaborators

  • Primus Pharmaceuticals

Registry information

Official study title

Safety Profile and Bone Efficacy of the Phytoestrogen Genistein in a Cohort of Osteopenic, Postmenopausal Women After Three Years of Treatment: a Follow-up Study

Important dates

Study start
2005
Primary completion
2006
Study completion
2006
First posted
Feb 29, 2008
Registry last updated
May 19, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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