University of Colorado Anschutz Medical Center, Clinical Translational Research Center and Exercise Research Laboratory
Aurora, Colorado, 80045, United States
NCT Number: NCT00608062
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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Notify Me18 year–70 year
Female
Interventional
Not applicable
Aurora, Colorado, 80045, United States
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
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
0.075mg/d starting on day 4 of the injections following testing time point two; continue for 3 days and retest (day 7)
Starting on day 4 of the injections following testing time point two; continue for 3 days and retest (day 7)
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
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.
Time frame: Baseline, day 4 of GnRHant and day 7 of GnRHant and estradiol or placebo treatment
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.
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.
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.
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.
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.
University of Colorado, Denver
Other
Biological Mechanisms of Arterial Stiffening With Age and Estrogen Deficiency
Acronym: SHAPE
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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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