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| Sponsor: | National Heart, Lung, and Blood Institute (NHLBI) |
|---|---|
| Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
| ClinicalTrials.gov Identifier: | NCT00000613 |
Purpose
To determine the acceptability and benefits of use of a dietary supplement of the phytoestrogen, genistein, versus placebo on heart disease risk factors, bone density, and psychosocial outcomes in postmenopausal women.
| Condition | Intervention | Phase |
|---|---|---|
|
Bone Diseases Cardiovascular Diseases Coronary Disease Depression Heart Diseases Myocardial Ischemia Osteoporosis Postmenopause |
Behavioral: dietary supplements Drug: genistein Behavioral: diet, soy proteins |
Phase II |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Double-Blind, Placebo Control |
| Study Start Date: | April 1997 |
| Estimated Study Completion Date: | December 2004 |
BACKGROUND:
Estrogen replacement therapy is beneficial for heart disease risk factors as well as for bone density. However, a large proportion of postmenopausal women are not compliant with therapeutic regimens. Phytoestrogens are naturally occurring compounds found in plants and soy products that have estrogenic effects, and may represent an alternative treatment for the prevention of heart disease and osteoporosis in postmenopausal women. However, few intervention trials have examined the extent to which it is possible to improve heart disease risk factors, bone density, and quality of life in postmenopausal women through use of a dietary supplement of phytoestrogen.
DESIGN NARRATIVE:
Randomized, double-blind, placebo-controlled study. A total of 210 women were enrolled in the study to be followed for one to two years. The women were randomized to phytoestrogen treatment or to placebo. Data are collected at baseline visits, at one and three month follow-up telephone calls, and at 6, 12, and 24 month follow-up clinic visits. Measures of high density lipoprotein and other heart disease risk factors, hip and spine bone density, and depression, life satisfaction, and quality of well-being are obtained. Cross-sectional and longitudinal comparisons of treatment and placebo groups are performed before and after adjustment and stratification for potentially confounding covariates.
The study was renewed in March 2002 to assess whether the women treated with phytoestrogens had lowered homocysteine, interleukin-6, C-reactive protein, E-selectin, and decreased obesity and fat mass over two years.
Eligibility| Ages Eligible for Study: | 45 Years to 74 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Postmenopausal women, ages 45 to 74.
Contacts and Locations
More Information
| Study ID Numbers: | 116 |
| Study First Received: | October 27, 1999 |
| Last Updated: | January 3, 2006 |
| ClinicalTrials.gov Identifier: | NCT00000613 History of Changes |
| Health Authority: | United States: Federal Government |
|
Anticarcinogenic Agents Molecular Mechanisms of Pharmacological Action Antineoplastic Agents Myocardial Ischemia Physiological Effects of Drugs Hormones, Hormone Substitutes, and Hormone Antagonists Arteriosclerosis Protein Kinase Inhibitors Bone Diseases Hormones Pathologic Processes Musculoskeletal Diseases Mental Disorders Therapeutic Uses Phytoestrogens |
Cardiovascular Diseases Arterial Occlusive Diseases Estrogens Heart Diseases Depression Vascular Diseases Osteoporosis Enzyme Inhibitors Bone Diseases, Metabolic Ischemia Depressive Disorder Protective Agents Pharmacologic Actions Behavioral Symptoms Coronary Disease |