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Menopause clinical trials

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NCT ID: NCT05715372 Terminated - Aging Clinical Trials

Genetic Evaluation and Modification of Lifestyles to Improve Female Life Expectancy

GEMLIFE
Start date: June 22, 2021
Phase: N/A
Study type: Interventional

The GEMLIFE Study is a 12-month clinical trial for menopausal women. The purpose of this study is to promote an improved aging process for women in menopause through lifestyle changes. The changes will include a heart healthy diet, structured walking program, and mindfulness-based stress reduction. During the study, the investigators will monitor components of your genetic make-up that will tell us how you are aging. Investigators will also monitor bloodwork for inflammation that can affect medical conditions. Study participants may qualify if you are within 5 years of your last menstrual period and have well controlled medical conditions. There is no cost to participants to enroll in the study- only potential benefits to the participant's health and aging process.

NCT ID: NCT04140968 Terminated - Menopause Clinical Trials

Progesterone and Resting Energy Expenditure

P4&REE
Start date: November 1, 2019
Phase: Phase 4
Study type: Interventional

This study evaluates the effect of micronized progesterone substitution in the luteal phase on resting energy expenditure in women during menopausal transition.

NCT ID: NCT03942276 Terminated - Hypertension Clinical Trials

Effects of Different Exercises Interventions in Post-menopausal Women

Start date: September 1, 2019
Phase: N/A
Study type: Interventional

This study will compare different exercise training protocols on health parameters of postmenopausal women. The hypothesis is that short duration high intensity interval training will promote different effects of long duration moderate intensity training.

NCT ID: NCT03642119 Terminated - Menopause Clinical Trials

Validation of an Objective Instrument to Measure Hot Flashes During Menopause

FLAME
Start date: September 7, 2018
Phase:
Study type: Observational

The overarching aim of this study is to assess the validity of the iButton®, a dual temperature and humidity sensing device (DS1923; Maxim IntegratedTM), as an objective method to assess hot flash incidence and dynamics in both a real world (ambulatory) and controlled (laboratory) setting. This study will test the overarching hypothesis that both self-report hot flashes in both an ambulatory and laboratory setting will correlate (confirm) the temperature and humidity sensing observed via the iButton® technology.

NCT ID: NCT03529838 Terminated - Hypertension Clinical Trials

Hemodynamic and Salivary Responses of 12 Weeks of Training With Different Anti-hypertensive

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Different classes of antihypertensives may have different responses when associated with exercise. Thus, this study aims to compare the responses of the association of 12 weeks of aerobic exercise and weightlifting with different classes of medications in 45 postmenopausal hypertensive women.

NCT ID: NCT03396978 Terminated - Menopause Clinical Trials

The Influence of Gonadal Hormone Suppression on Adipocyte Lineage and the Microbiome

BATE Plus
Start date: January 11, 2018
Phase: N/A
Study type: Interventional

This research study plans to learn more about the role of female sex hormones on adipose tissue (or fat) and the gut microbiome (or the organisms that are in your digestive tract). The rationale for this study is that the rate at which women gain fat (especially in the stomach region) increases after menopause. It is thought to be due to the loss of estrogen because post-menopausal women who take estrogen gain less weight than those who do not take estrogen. Gut bacteria process estrogen and help determine the types of estrogen that circulate in the body. These bacteria can be changed with lifestyle factors such as diet, and may therefore, also affect the risk of diseases that are more common in women after menopause i.e., cardiovascular disease and cancer. In this study the investigators will obtain fat biopsies before and after 6 months of ovarian hormone suppression to measure how the fat cells change with the loss of female sex hormones (e.g., medical menopause). The investigators will also obtain stool and urine samples before and every month during the study to measure changes in the microbiome.

NCT ID: NCT02775448 Terminated - Obesity Clinical Trials

Dose-response Study of Carduus Marianus in Centesimal Scale for Dyslipidemia in Climacteric Overweighed or Obese Women.

Start date: February 2016
Phase: Phase 2
Study type: Interventional

Metabolic disorders including hypercholesterolemia and hypertriglyceridemia are present in climacteric women. Carduus marianus is a homeopathic medicine that traditionally has been used for hepatic diseases. It has been used for reducing hypercholesterolemia and hypertriglyceridemia also. The aim of this study is to investigate the most effective dose of Carduus marianus in centesimal scale (6cH, 12cH, 30cH, placebo) plus diet and exercise for reducing hypertriglyceridemia and/or hypercholesterolemia in climacteric women.

NCT ID: NCT02693002 Terminated - Menopause Clinical Trials

Estrogen Diastolic Heart Failure

Start date: February 2016
Phase: Phase 4
Study type: Interventional

Peri-menopausal women will be randomized to hormone replacement therapy or placebo for 12 weeks to determine if markers of systolic and diastolic function change by echocardiography as well as laboratory markers of heart failure, including b-type natriuretic peptide (BNP).

NCT ID: NCT02497560 Terminated - Menopause Clinical Trials

A Study To Investigate The Effect Of A Natural Dietary Supplement On Peri-Menopausal Symptoms

Start date: March 2015
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized, masked, placebo controlled study to assess the effect on a nutritional dietary supplement on menopausal signs and symptoms in perimenopausal women.

NCT ID: NCT01633814 Terminated - Aging Clinical Trials

Hormone Replacement and Neural Cardiovascular Control in Postmenopausal Women

Start date: September 2011
Phase: N/A
Study type: Interventional

Older women have an exaggerated increase in blood pressure during exercise. However, the reasons for this are unclear. It is important to investigate this phenomenon because a greater blood pressure response to exercise has been associated with an increased risk of stroke and mortality in otherwise healthy individuals. A unique aspect of aging in women is the profound change in hormone levels (i.e. estrogen and progesterone) associated with menopause. The influence of changes in estrogen and progesterone levels on the cardiovascular responses to exercise is poorly understood. However, it has been suggested that these hormones might change the responsiveness of the cardiovascular system. Possible mechanisms that could account for these changes are the arterial baroreflex and feedback from the exercising muscle (known as the exercise pressor reflex), both of which are known to powerfully modulate blood pressure during exercise. However, to date, few human studies have thoroughly examined the influence of changes in hormone levels on baroreflex function during exercise or the exercise pressor reflex in older women. As such, the purpose of this research project is to assess baroreflex function and the exercise pressor reflex in older women after transdermal estrogen alone, transdermal estrogen plus progesterone, progesterone alone and placebo.