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Completed

NCT Number: NCT00608062

Sex Hormones and Atherosclerosis Prevention in Perimenopausal Women

The purpose of this study is to find out why women's arteries stiffen as they go through menopause, and how this is affected by estrogen loss. We believe that arteries stiffen with the loss of estrogen because of "oxidative stress," the production of molecules that can damage cells and tissues in the body, and because the arteries lose their ability to expand, or dilate.

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Key information

Age range

18 year–70 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of Colorado Anschutz Medical Center, Clinical Translational Research Center and Exercise Research Laboratory

Aurora, Colorado, 80045, United States

About this study

As women get older and go through menopause, estradiol levels decrease. Also with aging, the arteries that are located around the heart get stiffer. Over time this increase in arterial stiffness can lead to a number of health problems such as high blood pressure and heart disease. In this study we want to find out if a short-term drop in estrogen levels in premenopausal and perimenopausal women can cause arteries to become stiffer, and why this happens. Additionally, in postmenopausal women, we want to find out if a short-term increase in estrogen levels causes their arteries to become more flexible (less stiff).

Arterial health (i.e., stiffness) will be examined in premenopausal, perimenopausal and postmenopausal women before and after they are given a drug called Ganirelix™ (for 7 days), which will markedly lower their reproductive hormones. After the first 4 days of taking Ganirelix™, the women will be randomly placed into 1 of 2 treatment groups to take either estrogen (0.075 mg/d skin patch) replacement or placebo for the rest of the Ganirelix treatment. This is to increase estrogen levels back to the normal level. After having the patch on for 4 days, arterial health will be examined again.

Pre-specified Outcome Measures were divided into unit-of-measurement specific Outcome Measure tables for the purposes of results reporting to ClinicalTrials.gov

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy women of all races and ethnic backgrounds in one of the following groups:
  • Premenopausal: 18-49 years, regular menstrual cycles with no change in observed cycle length (21-35 days)
  • Perimenopausal: 40-55 years, categorized as either early (at least 2 cycles with cycle length changes of at least 7 days) or late (more than 3 months of amenorrhea) transition
  • Postmenopausal: 45-70 years, more than 12 months of amenorrhea as defined by the menopausal staging system (STRAW); additionally, postmenopausal women will be categorized into early and late stages as defined by the STRAW definition, specifically, women who are less than 5 years postmenopause will be considered early, and women more than 6 years will be categorized as late
  • All postmenopausal women will have undergone natural menopause
  • No oral contraceptive or Hormone Replacement Therapy (HRT) use for at least 6 months
  • Resting blood pressure less than 140/90 mmHg
  • Plasma glucose concentrations less than 110 mg/dl under fasting conditions
  • Sedentary or recreationally active (less than 3 days of vigorous aerobic exercise)
  • No use of medications that might influence cardiovascular function
  • Nonsmokers
  • No use of vitamin supplements or willing to stop use for duration of the study

Exclusion criteria

  • History of or active estrogen-dependent neoplasms, acute liver or gallbladder disease, vaginal bleeding, venous thromboembolism, hypertriglyceridemia, and cardiovascular disease
  • Known allergy to transdermal patch or GnRHant
  • Other contraindications to HRT and GnRHant

Treatment and study plan

GnRHant - Ganirelix acetate

Drug

1 subcutaneous injection at 0.5 mg then daily injections of 0.25 mg for 6 days (total of 7 days of injections); testing will occur on injection day 4 and day 7

Other names: Ganirelix

Transdermal estradiol patch

Drug

0.075mg/d starting on day 4 of the injections following testing time point two; continue for 3 days and retest (day 7)

Transdermal Placebo Patch

Drug

Starting on day 4 of the injections following testing time point two; continue for 3 days and retest (day 7)

Primary outcomes

  1. Arterial Stiffness (Carotid Artery Compliance) During Saline

    Time frame: Baseline, day 4 of GnRHant and day 7 of GnRHant and estradiol or placebo treatment

    Carotid artery compliance measured by carotid artery ultrasound and brachial artery blood pressure

  2. Endothelial Function

    Time frame: Baseline, day 4 of GnRHant and Day 7 of GnRHant and estradiol or placebo treatment

    Brachial artery flow-mediated dilation (FMD) assessed by ultrasound. This other outcome measure was originally specified as "Secondary" in error and has been updated to "Primary" to be consistent with the protocol.

Other outcomes

  1. Supine Brachial Blood Pressures

    Time frame: Baseline, day 4 of GnRHant and day 7 of GnRHant and estradiol or placebo treatment

  2. Estradiol

    Time frame: Baseline, day 4 of GnRHant and day 7 of GnRHant and estradiol or placebo treatment

    This other outcome measure was originally specified as "Secondary" in error and has been updated to "Other, Pre-specified" to be consistent with the protocol. Serum estradiol for clinical characteristics and to detect changes in estradiol levels with the interventions.

  3. Progesterone

    Time frame: Baseline, Day 4 GnRHant, Day 7 GnRHant+Add-back

    This other outcome measure was originally specified as "Secondary" in error and has been updated to "Other, Pre-specified" to be consistent with the protocol. Serum progesterone was measured for clinical characteristics and to determine changes in sex hormones.

  4. Total Antioxidant Status (TAS)

    Time frame: Baseline, Day 4 GnRHant, Day 7 GnRHant+Add-back

    This other outcome measure was originally specified as "Secondary" in error and has been updated to "Other, Pre-specified" to be consistent with the protocol. TAS is an antioxidant and is a biomarker of oxidative stress.

  5. Endothelin-1 (ET-1)

    Time frame: Baseline, Day 4 GnRHant, Day 7 GnRHant+Add-back

    This other outcome measure was originally specified as "Secondary" in error and has been updated to "Other, Pre-specified" to be consistent with the protocol.

  6. Plasma Norepinephrine

    Time frame: Baseline, Day 4 GnRHant, Day 7 GnRHant+Add-back

    This other outcome measure was originally specified as "Secondary" in error and has been updated to "Other, Pre-specified" to be consistent with the protocol.

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Collaborators

  • National Institute on Aging (NIA)

Registry information

Official study title

Biological Mechanisms of Arterial Stiffening With Age and Estrogen Deficiency

Acronym: SHAPE

Important dates

Study start
2007
Primary completion
2012
Study completion
2012
First posted
Feb 6, 2008
Registry last updated
Dec 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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