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Sponsored by: |
National Heart, Lung, and Blood Institute (NHLBI) |
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Information provided by: | National Heart, Lung, and Blood Institute (NHLBI) |
ClinicalTrials.gov Identifier: | NCT00041431 |
To determine the effects of estrogen therapy on postmenopausal women with congestive heart failure.
Condition | Intervention |
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Cardiovascular Diseases Heart Failure, Congestive Heart Diseases Menopause |
Drug: Hormone Replacement Therapy |
Study Type: | Interventional |
Study Design: | Randomized, Double-Blind, Placebo Control |
Study Start Date: | December 2001 |
Estimated Study Completion Date: | December 2003 |
BACKGROUND:
Congestive heart failure (CHF) is a leading cause of morbidity, mortality, and hospitalization in women. The increase in mortality suggests that postmenopausal estrogen loss may alter the phenotypic expression of CHF. Because estrogen is a potent in vitro inhibitor of pro-inflammatory cytokines (e.g., TNFa, IL-1B, IL-6), which are re-expressed by the failing myocardium in patients with CHF and are related to an adverse prognosis, the study postulates that estrogen replacement will improve the outcome of postmenopausal women with CHF.
DESIGN NARRATIVE:
The randomized, double blind study was conducted in 166 postmenopausal women with congestive heart failure due to idiopathic (i.e.nonischemic) dilated cardiomyopathy and NYHA class II or III symptoms on either combined estrogen and progestin or placebo. Women maintained their then current congestive heart failure medications for six months. Three outcomes were measured: 1) Congestive heart failure severity/functional capacity quantified by maximum oxygen consumption during metabolic stress testing; 2) Left and right ventricular remodeling quantified by electron bean CT scan; 3) quality of life assessment by the Minnesota Living with Heart Failure and Kansas City cardiomyopathy questionnaires. In addition, measurements were made of pro-inflammatory markers, that had been demonstrated to be elevated in congestive heart failure to assess whether hormone replacement therapy reduced them.
Genders Eligible for Study: | Female |
Accepts Healthy Volunteers: | No |
Postmenopausal women with NYHA Class II or Class III congestive heart failure due to idiopathic dilated cardiomyopathy.
Study ID Numbers: | 1181 |
Study First Received: | July 8, 2002 |
Last Updated: | June 23, 2005 |
ClinicalTrials.gov Identifier: | NCT00041431 History of Changes |
Health Authority: | United States: Federal Government |
Estrogens Heart Failure Heart Diseases Hormones Menopause |
Heart Failure Heart Diseases Cardiovascular Diseases |