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Postmenopausal Disorder clinical trials

View clinical trials related to Postmenopausal Disorder.

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NCT ID: NCT03672760 Recruiting - Vascular Stiffness Clinical Trials

Inspiratory Muscle Training X CardioBreath App Effects On Vagal Modulation And Pulse Wave Velocity

CardioBreath
Start date: September 1, 2023
Phase: N/A
Study type: Interventional

Existing data points to relevant beneficial effects of respiratory exercises on cardiovascular health, with special regards to decreases on arterial pressure and improves on autonomic and vascular profiles, though mechanistics of such results have not yet been cleared. Among the available ways to perform respiratory exercises, there is the highly recommended Inspiratory Muscle Training (IMT) and slow breathing exercises like Yoga pranayamas. Lately, the development of new technologies has allowed the use of Apps to perform respiratory exercises. This study will be take the just developed CardioBreath®App to validate it as a tool to perform respiratory exercises. Therefore, it will be compared to IMT on cardiac vagal modulation and pulse wave velocity on normotensive post menopause women.

NCT ID: NCT03469518 Active, not recruiting - Osteoporosis Clinical Trials

Effect of β-cryptoxanthin (β-Cx), Plant Sterols and Galactooligosaccharides on Systemic and Gastrointestinal Markers

Start date: January 2017
Phase: N/A
Study type: Interventional

Regular consumption of a beverage containing β-cryptoxanthin (β-Cx) and plant sterols (PS) has been shown to exert a synergic effect in reducing some markers of cardiovascular risk and bone-remodeling (formation and resorption). The present project aims to: - Evaluate (by in vivo and in vitro studies) the bioavailability of added β-Cx, PS and galactooligosaccharides (GOS) and its stability in the beverage employed in the proposed study. - Study the biological effect (bioefficacy) associated with the regular consumption of modified milk-based fruit beverages containing β-Cx, PS and GOS in post-menopausal women (target group) by assessing changes in inflammation, cardiovascular and bone turnover biochemical markers. - Characterize genetic variability (polymorphisms), genetic expression and DNA oxidative damage in the target group as determinants of bioavailability and biological effects of β-Cx, PS and GOS. - Evaluate the potential prebiotic effect associated to regular consumption of a beverage supplemented with β-Cx, PS and GOS: including "in vitro" studies and characterization of subjects' microbiota and possible microbiota changes associated to the beverage consumption.

NCT ID: NCT03295487 Completed - Clinical trials for Stress Urinary Incontinence

ToT and Estrogen in Postmenopausal Females

Start date: March 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

To compare the subjective and objective outcomes of TVT-O procedure alone versus the same procedure followed by the use of premarin vaginal cream for 3 months in postmenopausal female with genuine stress incontinence.

NCT ID: NCT03280693 Completed - Osteoporosis Clinical Trials

Relationships Among Body Mass Index, Body Balance and Bone Mineral Density in Postmenopausal Women

Start date: May 2015
Phase: N/A
Study type: Observational

Body composition, bone mineral density (BMD), and body balance are important factors that threaten postural control. They act as vital elements in the vicious circle that leads to fracture occurrence in elderly population, particularly postmenopausal women.

NCT ID: NCT03233932 Completed - Clinical trials for Postmenopausal Disorder

CKD-841 Pharmacokinetic/Pharmacodynamic Study

Start date: April 2016
Phase: Phase 1
Study type: Interventional

A randomized, open-label, single dose, parallel design phase I clinical trial to investigate the safety and pharmacokinetic/pharmacodynamics of CKD-841 or Leuplin Inj. 3.75mg after subcutaneous injection in postmenopausal female.

NCT ID: NCT01833663 Completed - Overactive Bladder Clinical Trials

Effectiveness and Safety Study of Solifenacin Succinate and Solifenacin Succinate + Estrogen to Treat OAB in Postmenopausal Women

OAB
Start date: October 2011
Phase: Phase 4
Study type: Interventional

This study is a multi-site, randomized, opened and parallel-controlled clinical study. The patients up to the inclusion criteria are randomly treated with Solifenacin Succinate Tablets (5mg/d) or Solifenacin Succinate Tablets (5mg/d) + local estrogen for 12 weeks. Before the dosing and at Week 4, 8 and 12 of the dosing, various examinations are made, and various indices are evaluated.

NCT ID: NCT01745042 Completed - Clinical trials for Postmenopausal Disorder

Anthropometric, Metabolic, Cardiovascular and Symptomatic Profile in Postmenopausal Women

Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to investigate anthropometric, metabolic, cardiovascular and symptomatic profiles in postmenopausal women.

NCT ID: NCT01519583 Completed - Blood Pressure Clinical Trials

WalkMore Walking Interventions for Overweight/Obese Postmenopausal Women

Start date: May 2012
Phase: N/A
Study type: Interventional

The WalkMore study will help find out how walking interventions can help overweight/obese postmenopausal women with increased risk of cardiovascular disease lower their blood pressure.

NCT ID: NCT01400724 Completed - Metabolic Syndrome Clinical Trials

Inofolic NRT and the Metabolic Syndrome

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

A prospective, randomized, controlled, open-label study will be carried out on 80 post-menopausal women affected by the metabolic syndrome (criteria are described in NIH ATP III). After a written informed consent, women will be randomly treated for 6 months with hypocaloric diet (control group) or with diet and a supplementation of myo-inositol 2000 mg plus cocoa polyphenols 30 mg and plus isoflavones 80 mg. will be given randomly Eighty post-menopausal women, affected by metabolic syndrome will be randomized into two groups: 40 treated with myo-inositol 2 g twice per day and forty treated with placebo for six months. The investigators hypothesize that the administration of myo-inositol would improve the insulin-receptor activity in these women, reducing insulin resistance.

NCT ID: NCT01398605 Completed - Clinical trials for Postmenopausal Disorder

Physical Activity in Postmenopausal Women

Start date: September 2008
Phase: N/A
Study type: Interventional

The study is designed to investigate the physical activity and its dose-response relationship in postmenopausal women on the cardiovascular risks and cardiac function.