Full Text View
Tabular View
No Study Results Posted
Related Studies
ELITE: Early Versus Late Intervention Trial With Estradiol
This study is currently recruiting participants.
Verified by National Institute on Aging (NIA), August 2008
First Received: June 15, 2005   Last Updated: August 21, 2008   History of Changes
Sponsor: National Institute on Aging (NIA)
Information provided by: National Institute on Aging (NIA)
ClinicalTrials.gov Identifier: NCT00114517
  Purpose

The purpose of this study is to examine the effects of 17B-estradiol (estrogen) on the progression of early atherosclerosis in postmenopausal women.


Condition Intervention Phase
Atherosclerosis
Drug: 17B-estradiol
Phase II
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Factorial Assignment, Efficacy Study
Official Title: Biologic Response of Menopausal Women to 17B-Estradiol

Resource links provided by NLM:


Further study details as provided by National Institute on Aging (NIA):

Primary Outcome Measures:
  • rate of change of distal common carotid artery (CCA) far wall intima-media thickness (IMT)

Secondary Outcome Measures:
  • neurocognitive function

Estimated Enrollment: 504
Study Start Date: July 2004
Estimated Study Completion Date: June 2009
Detailed Description:

The primary hypothesis to be tested is that 17B-estradiol (estrogen) will reduce the progression of early atherosclerosis if initiated soon after menopause when the vascular endothelium (lining of blood vessels) is relatively healthy versus later when the endothelium has lost its responsiveness to estrogen. Ultrasonography will be used to measure the rate of change in the thickness of the carotid artery.

A total of 504 postmenopausal women will be randomized according to their number of years since menopause, less than 6 years or 10 years or more, to receive either oral 17B-estradiol 1 mg daily or a placebo. Women with a uterus will also use vaginal progesterone gel 4% (or a placebo gel) the last ten days of each month. The vaginal progesterone will be distributed in a double-blind fashion along with the randomized treatment so that only women exposed to active treatment will receive active progesterone. Participants will receive ultrasonography at baseline and every 6 months throughout the 2 to 5 years (average 3 years) of randomized treatment.

  Eligibility

Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Women with a serum estradiol level 25 pg/ml or less
  • No period for 6 months or more
  • Postmenopausal less than 6 years, OR 10 years or longer

Exclusion Criteria:

  • Clinical signs, symptoms, or personal history of cardiovascular disease
  • Women who have had a hysterectomy only and no oophorectomy (since time from menopause cannot be determined)
  • Diabetes mellitus or fasting serum glucose 140 mg/dL or greater
  • Uncontrolled hypertension (diastolic blood pressure 110 mmHg or greater)
  • Thyroid disease (untreated)
  • Serum creatinine greater than 2.0 mg/dL
  • Plasma triglyceride levels greater than 500 mg/dL
  • Life threatening disease with prognosis less than 5 years
  • Cirrhosis or liver disease
  • History of deep vein thrombosis or pulmonary embolism
  • History of breast cancer
  • Current hormone replacement therapy (HRT)
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00114517

Locations
United States, California
Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine Recruiting
Los Angeles, California, United States, 90033
Contact: Howard N. Hodis, MD     866-240-1489     aru@usc.edu    
Sponsors and Collaborators
Investigators
Principal Investigator: Howard N. Hodis, MD University of Southern California, Atherosclerosis Research Unit, Division of Cardiovascular Medicine, Department of Medicine
  More Information

Additional Information:
No publications provided

Responsible Party: USC ( Howard N. Hodis, MD )
Study ID Numbers: AG0025, R01AG024154
Study First Received: June 15, 2005
Last Updated: August 21, 2008
ClinicalTrials.gov Identifier: NCT00114517     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Institute on Aging (NIA):
cardiovascular disease
CVD
estrogen
bone density
cognitive function
postmenopausal

Additional relevant MeSH terms:
Atherosclerosis
Arterial Occlusive Diseases
Estrogens
Contraceptive Agents
Physiological Effects of Drugs
Estradiol valerate
Contraceptive Agents, Female
Vascular Diseases
Hormones, Hormone Substitutes, and Hormone Antagonists
Reproductive Control Agents
Arteriosclerosis
Estradiol 17 beta-cypionate
Hormones
Pharmacologic Actions
Estradiol
Therapeutic Uses
Estradiol 3-benzoate
Cardiovascular Diseases
Polyestradiol phosphate

ClinicalTrials.gov processed this record on November 27, 2009