|
Home
Search
Study Topics
Glossary
|
![]() |
![]() |
|
![]() |
|
![]() |
|
![]() |
![]() |
![]() |
|
![]() |
![]() |
||||||||||||||||||||||||||||||||||||
| 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: | Allocation: Randomized Masking: Double-Blind Primary Purpose: Prevention |
| 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
| ClinicalTrials.gov Identifier: | NCT00000613 History of Changes |
| Other Study ID Numbers: | 116 |
| Study First Received: | October 27, 1999 |
| Last Updated: | January 3, 2006 |
| Health Authority: | United States: Federal Government |
|
Bone Diseases Cardiovascular Diseases Myocardial Ischemia Coronary Artery Disease Coronary Disease Depression Depressive Disorder Heart Diseases Ischemia Osteoporosis Musculoskeletal Diseases Vascular Diseases Arteriosclerosis Arterial Occlusive Diseases Behavioral Symptoms |
Mood Disorders Mental Disorders Pathologic Processes Bone Diseases, Metabolic Genistein Phytoestrogens Estrogens, Non-Steroidal Estrogens Hormones Hormones, Hormone Substitutes, and Hormone Antagonists Physiological Effects of Drugs Pharmacologic Actions Anticarcinogenic Agents Protective Agents Antineoplastic Agents |