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Completed

NCT Number: NCT00665860

Safety and Effectiveness of Soy Phytoestrogens to Prevent Bone Loss

The purpose of this study is to determine whether soy isoflavone supplementation is safe and effective to prevent bone loss in postmenopausal women.

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Key information

Age range

40 year–60 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Davis, California, United States

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About this study

Over-the-counter soy isoflavone supplement usage is becoming common among postmenopausal women. However, there is no documented scientific evidence of its long-term safety and efficacy in preventing osteoporosis. Our primary goal is to determine the safety, efficacy, and optimal dosage of isoflavone supplementation to reduce bone loss in postmenopausal women. The multi-state, multi-institutional design ensures that the study results are representative of postmenopausal women in the U.S. population. Confirming the skeletal benefits of soy isoflavones could translate into reduced healthcare costs related to osteoporosis.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Must be able to swallow the pills
  • No menses for 12 months
  • Blood follicle stimulating hormone great than 30 IU/mL
  • Lumbar spine bone mineral density t-score equal to or greater than -1.5

Exclusion criteria

  • Strict vegetarians
  • Current or recent smokers (within last five years)
  • Abnormal screening mammogram, Pap smear and blood chemistries
  • Clinical diagnosis of osteoporosis, spine and/or hip fracture, cancer, liver, kidney, gallbladder and heart disease
  • Clinical diagnosis of psychiatric disorder
  • Any allergic reactions to soy products
  • Current treatment with bisphosphonates, calcitonin, fluoride, corticosteroids, tamoxifen, raloxifene, HRT, premarin, farestron and letrozole
  • Current usage of black cohosh, blue cohosh, dong quai, Caltrate 600+Soy, Estroven, ginseng, Healthy Women, Natural Estrogen, Opti-Soy, PhytoFem, Probalance, Promensil, Remifemin, Rimostil and Trinovin

Treatment and study plan

Placebo

Dietary Supplement

Three pills per day for two years

Soy isoflavones

Dietary Supplement

Three pills that delivered 80 mg of aglycone isoflavones per day for two years

Other names: Soy germ isoflavones

Primary outcomes

  1. Bone mineral density

    Time frame: One year and two years

Secondary outcomes

  1. Blood biochemical bone markers (osteocalcin, bone-specific alkaline phosphatase, cross-linked N-telopeptides of type 1 collagen)

    Time frame: One year and two years

Sponsors and collaborators

Lead sponsor

Baylor College of Medicine

Other

Collaborators

  • Kaiser Foundation Research Institute
  • Texas A&M University
  • University of Alabama at Birmingham
  • University of California
  • University of Georgia

Registry information

Official study title

Safety, Efficacy, and Optimal Dosage of Soy Isoflavones to Prevent Osteoporosis

Acronym: OPUS

Important dates

Study start
2001
Primary completion
2006
Study completion
2006
First posted
Apr 24, 2008
Registry last updated
Nov 27, 2020

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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