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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02256540
Other study ID # 14-0532
Secondary ID UL1TR001082R56HL
Status Completed
Phase N/A
First received
Last updated
Start date August 2014
Est. completion date March 25, 2016

Study information

Verified date March 2020
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This pilot study plans to learn more about the aging of blood vessels and arteries in women. As women age and go through menopause, their risk for cardiovascular disease increases. Also with aging and menopause, levels of the reproductive hormone estradiol decline. Hormone replacement therapy to restore estradiol levels does not protect women from cardiovascular disease, so lifestyle changes, such as regular exercise, are recommended to reduce disease risk. However, there are differences between men and women in their response to exercise. In older men, exercise improves the health of their arteries, but in postmenopausal women, exercise does not provide this benefit. The purpose of this pilot study is to determine whether low estradiol levels in postmenopausal women are responsible for the poor vascular response to exercise. In this study the investigators will also test whether treatment with resveratrol, a plant compound found in red wine, improves postmenopausal women's response to exercise. The investigators hypothesize that acute treatment with estrogen or resveratrol will improve vascular responses to an acute bout of exercise.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date March 25, 2016
Est. primary completion date March 25, 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 50 Years to 70 Years
Eligibility Inclusion Criteria:

- Between the ages of 50-70 and at least 1 year beyond menopause;

- resting blood pressure <140/90 mmHg;

- plasma glucose concentrations <110 mg/dL under fasting conditions;

- BMI < 35;

- LDL cholesterol < 160 mg/dL;

- sedentary or recreationally active (<3 days of vigorous aerobic exercise);

- no use of OCs, HT, or other medications that might influence cardiovascular function;

- nonsmokers;

- no use of vitamin supplements, blood thinners or NSAIDS, or willing to stop use one month prior to and for the duration of the study;

- not taking any other medications that would interact with E2 patch or resveratrol to confound interpretation of results.

Exclusion Criteria:

- history of or active E2-dependent neoplasms, acute liver or gallbladder disease, vaginal bleeding, venous thromboembolism, hypertriglyceridemia (= 150 mg/dL), and CVD;

- known allergy to transdermal patch, or resveratrol;

- history of stomach ulcer or bleeding;

- other contraindications to HT or resveratrol.

- other conditions for which individuals will be excluded from the study include: diabetes, active infection, history of seizures or disease that affects the nervous system or an abnormal resting ECG.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Climara

Placebo patch
Placebo patch designed to match active Climara patches.
Dietary Supplement:
Resveratrol

Placebo
Placebo tablets designed to match active resveratrol tablets.

Locations

Country Name City State
United States University of Colorado Anschutz Medical Campus Aurora Colorado

Sponsors (2)

Lead Sponsor Collaborator
University of Colorado, Denver National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change in Brachial Artery Flow-mediated Dilation at Each Time Point Brachial artery flow-mediated dilation represents the percent change in artery diameter (before and after blood pressure cuff inflation-deflation) within each time point. Up to 2 hours post-exercise
Secondary Gene and Protein Expression in Peripheral Blood Mononuclear Cells No gene and protein data were analyzed. baseline, 1-2 hours post-exercise
Secondary Change in Nitrate/Nitrite Levels Measure of nitric oxide baseline, 1-2 hrs post-exercise
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