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临床试验/NCT00076050
NCT00076050已完成3 期

Bone Sparing Effects of Soy Phytoestrogens in Menopause

University of Miami1 个研究点 分布在 1 个国家目标入组 248 人开始时间: 2003年9月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
248
试验地点
1
主要终点
Change From Baseline in Bone Mineral Density

研究概览

简要总结

The purpose of this study is to determine if soy-derived phytoestrogens (naturally occurring compounds similar to estrogen) can prevent bone loss and other menopausal symptoms in women who have recently gone through menopause.

Study hypothesis: Tablets of high-dose, purified soy phytoestrogens spare the normally occurring spinal bone loss and improve biological and other emotional changes of menopause.

详细描述

The risks of bone loss and osteoporosis increase significantly after menopause. Although hormone therapy (HT) can spare menopausal women from bone loss and other menopausal symptoms, Women's Health Initiative (WHI) findings indicate significant potential health risks associated with HT. This has prompted women to switch from HT to naturally occurring compounds similar to estrogen, such as those derived from soy, in the hope that estrogens from plant sources can provide benefits while sparing adverse effects caused by prescribed estrogens. However, the long-term efficacy and safety of plant estrogens are unknown. This study will evaluate the effectiveness of treatment using purified soy isoflavones, a dietary source of phytoestrogens, in preventing bone loss, menopausal symptoms, and other changes associated with estrogen deficiency in young menopausal women. The "Soy Phytoestrogens As Replacement Estrogen (SPARE)" study will provide a foundation of knowledge from which menopausal women and their doctors can begin to make more informed decisions regarding HT and other treatment options.

Enrollment into the study will occur over 3 years, with each participant taking part in the study for a total of 2 years. Participants will be randomly assigned to one of two groups; the first group will receive a 200 mg dose of soy isoflavones daily and the second group will receive placebo daily. There will be 10 study visits: screening, study entry, randomization at Month 1, six follow-up visits at Months 2, 4, 8, 12, 16, 20, and a final visit at the end of active participation at Month 24. At each study visit, participants will have blood drawn, provide urine samples, answer questionnaires, and have mammograms and bone density tests.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
45 Years 至 60 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •Absence of menstrual period for 12 months but not more than 5 years, or absence of menstrual period for 6 to 12 months and follicle stimulating factor (FSH) greater than 40 IU/L

排除标准

  • •Treatment with estrogens, progesterone, raloxifene, or tamoxifen
  • •Treatment with bisphosphonates, calcitonin, fluoride, or systemic corticosteroids
  • •Use of soy/herbal supplements, including DHEA, within 3 months prior to study entry
  • •Use of antibiotics in the month prior to study entry
  • •Use of prescription medication to treat hot flashes
  • •Chemical menopause, including post-chemotherapy
  • •Hyperthyroidism
  • •Hypothyroidism
  • •Uncontrolled diabetes
  • •Malabsorption syndromes or other chronic diseases
  • •Body mass index (BMI) less than 20 or greater than 32
  • •Bone mineral density (BMD) T-score below -2.0 in lumbar spine or femoral neck

研究组 & 干预措施

2

Placebo Comparator

Participants will receive placebo daily over 2 years.

干预措施: Placebo (Dietary Supplement)

1

Experimental

Participants will receive a 200-mg dose of soy isoflavones daily over 2 years.

干预措施: Soy isoflavones (Dietary Supplement)

结局指标

主要结局

Change From Baseline in Bone Mineral Density

时间窗: baseline and 2 years

次要结局

  • Changes in Women's Health Questionnaire Score(baseline and 2 years)
  • Change in Vaginal Maturation Value(baseline and 2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Silvina Levis, MD

Professor

University of Miami

研究点 (1)

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