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Reduction of Triglycerides in Women on HRT - Article


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Ethinyl Estradiol and Norethindrone Acetate (Hormone Replacement Therapy)

Femhrt



Clinical Trial: Reduction of Triglycerides in Women on HRT

This study is currently recruiting patients.

Sponsored by: National Heart, Lung, and Blood Institute (NHLBI)
Information provided by: National Heart, Lung, and Blood Institute (NHLBI)

Purpose

To test the effect of lifestyle intervention on subclinical cardiovascular disease measures in women taking HRT.

Condition Treatment or Intervention
Cardiovascular Diseases
Atherosclerosis
Postmenopause
Heart Diseases
 Behavior: diet, fat-restricted
 Behavior: exercise
 Drug: hormone replacement therapy
 Drug: estrogen replacement therapy

MedlinePlus related topics:  Heart Diseases;   Heart Diseases--Prevention;   Vascular Diseases

Study Type: Interventional
Study Design: Prevention, Randomized

Further Study Details: 

Study start: September 2001;  Expected completion: August 2006

BACKGROUND: Cardiovascular disease is a common cause of morbidity and mortality in older women. Better methods of prevention via health promotion are needed. Estrogen hormone replacement therapy (HRT) may beneficially affect women's cardiovascular health, based on evidence from observational studies, but recent trial evidence suggests HRT may actually lead to increased risk of cardiovascular disease in new users. Understanding this untoward effect of HRTand how to prevent it is a significant aim.

DESIGN NARRATIVE: Randomized trial of 500 women on HRT for at least two years, aged 52-60 years, and three or more years postmenopausal to test whether reduction in waist circumference, triglycerides, dense low density lipoprotein cholesterol (LDLc), number of LDL particles, C-reactive protein, plasminogen activator inhibitor-I ( PAI-I) by aggressive diet exercise, versus a health education control will decrease progression or result in regression of measures of subclinical vascular disease. The intervention is designed to reduce total fat intake to 17 percent of calories, 1300 kilo calories, and increase moderate activity to 150-240 minutes per week to obtain a 10 percent reduction in weight. The primary endpoint will be a 20 percent or at least a 20 mg decrease in triglyceride levels, a 5 cm decrease in waist circumference, and a 10 percent decrease in LDLc. This will result in changes in subclinical measurements including carotid ultrasound, electron beam computer tomography of the coronary and aorta, pulse wave velocity, endothelial function, and tonometry of the radial artery. Nuclear magnetic resonance spectroscopy of lipoproteins, inflammatory markers, and estrogen metabolites will also be evaluated.

Eligibility

Ages Eligible for Study:  52 Years   -   60 Years,  Genders Eligible for Study:  Female

Criteria

No eligibility criteria

Location and Contact Information


Pennsylvania
      University of Pittsburgh, Pittsburgh,  Pennsylvania,  15261,  United States; Recruiting
Lewis H. Kuller, M.D., D.P.H.  412-624-3054    KULLER+ @PITT.EDU 
Lewis H. Kuller,  Study Chair

Study chairs or principal investigators

Lewis Kuller,  University of Pittsburgh   

More Information

Study ID Numbers:  981
Record last reviewed:  December 2004
Last Updated:  December 13, 2004
Record first received:  September 7, 2001
ClinicalTrials.gov Identifier:  NCT00023543
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08


Source: ClinicalTrials.gov
Cache Date: April 9, 2005


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November 18, 2008



Page Updated: June 1, 2005
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