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Menopause clinical trials

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NCT ID: NCT03236896 Completed - Menopause Clinical Trials

Studying the Impact of Exercise on Hot Flashes

Start date: October 2015
Phase: N/A
Study type: Interventional

A prospective randomized pragmatic trial will be used to obtain data on energy expenditure, temperature changes and vasomotor symptoms at baseline, during the intervention in which participants will be randomized to either exercise or to not exercise, and at the end of the 12-week intervention.

NCT ID: NCT03221816 Completed - Menopause Clinical Trials

Effect of Polyvitaminics (Pyridoxine Hydrochloride, Folic Acid and Cyanocobalamin) in the Concentration of Homocysteine and Lipid Profile in Postmenopausal Women: a Randomized Controlled, Double-blind Clinical Trial

Start date: December 2008
Phase: Phase 4
Study type: Interventional

Introduction: Cardiovascular diseases (CVD) are the main cause of death in Western countries. High levels of homocysteine (He) has been considered an important risk factor for coronary artery disease. Objective: To evaluate the effects of the drug Tenavit® (pyridoxine hydrochloride 4.00mg + folic acid 0.80mg + cyanocobalamin 0.40 mg) on plasma homocysteine concentrations and lipid profile in postmenopausal women. Methods: Sixty women were postmenopausal selected from the outpatient Gynecology Hospital Santa Marcelina that passed by routine consultations and fulfilling the inclusion criteria were invited to the study. The women were randomly allocated to control or experimental group (30 in each group) in a do uble-blind controlled clinical trial. The experimental group received one tablet of Tenavit® daily and the placebo group received the same tablet with the organoleptic characteristics of Tenavit® for a period of 4 months. The women were assessed before the intervention and after 4 months of medication. A self-report questionnaire to assess quality of life (QSF-36) was applied and anthropometric measurements, cholesterol and fractions, triglycerides, fasting glucose, homocysteine and cysteine were evaluated. Results: The only variable that presented significant alteration in both dimensions (between and within group) was the homocysteine. It was observed statistical significant between groups in the final measure for homocysteine (control group: 11.5mmol/ L; experimental group: 9.4 mmo

NCT ID: NCT03220672 Completed - Menopause Clinical Trials

Effectiveness of Assessment and Educational Intervention on Motor Control of the Pelvic Floor Muscle in Women

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

The goal of the present study is to evaluate the short and long term effectiveness of a tailored assessment and educational intervention on motor control of the pelvic floor muscle in menopausal and non-menopausal women.

NCT ID: NCT03218085 Completed - HIV/AIDS Clinical Trials

Role of Exogenous and Endogenous Sex Hormones on Tenofovir and Emtricitabine Disposition in Female Genital Tract

Start date: July 14, 2017
Phase:
Study type: Observational

Cervical biopsies will be collected from women aged 18 and over whom are virally suppressed and taking tenofovir as part of their antiretroviral therapy regimen. Blood plasma, peripheral blood mononuclear cells (PBMC), and cervicovaginal swabs will also be collected. Drug concentrations, hormone concentrations, inflammatory cytokines, and vaginal microbiome will be evaluated to understand the role of hormones, inflammation, and the microbiome in modulating drug efficacy in the female genital tract.

NCT ID: NCT03200639 Completed - Physical Activity Clinical Trials

Cachexia in Gynecological Cancer and the Preventive Role of Weight Training

Start date: May 30, 2015
Phase: N/A
Study type: Interventional

The study aim was to compare the effectiveness of combined training (CT; aerobic + resistance exercises) and high-intensity interval body weight training (HIITBW) on body composition, metabolic and inflammatory profile, physical function and quality of life in older women with gynecological and breast cancer and their pair-matched controls (older women with no cancer). The hypothesis of the present clinical trial is that HIITBW is effective as well as CT for improvements on body composition, metabolic and inflammatory profile, physical function and quality of life in older women with gynecological and breast cancer.

NCT ID: NCT03192176 Completed - Menopause Clinical Trials

A Dose-ranging Study of the Efficacy of ESN364 in Postmenopausal Women Suffering Vasomotor Symptoms (Hot Flashes)

Start date: July 19, 2017
Phase: Phase 2
Study type: Interventional

This study determined the effects of different doses and dosing regimens of ESN364 on the frequency and severity of hot flashes. The treatment was administered for 12 weeks to postmenopausal women, aged 40 to 65, suffering at least 50 moderate to severe hot flashes per week.

NCT ID: NCT03178695 Completed - Infertility Clinical Trials

Inovium Ovarian Rejuvenation Trials

Start date: June 1, 2017
Phase: Phase 1
Study type: Interventional

The Inovium Ovarian Rejuvenation Treatment is a PRP-based autologous treatment used in combination with a stimulated IVF sequence and Pre-Implantation Genetic Screening to treat infertility in women experiencing menopause, perimenopause, and premature ovarian failure.

NCT ID: NCT03126773 Completed - Menopause Clinical Trials

A Prospective Multicenter Study on Patients'Satisfaction With Angeliq® Micro in Real Clinical Practice Conducted in Russia

Start date: May 2, 2017
Phase:
Study type: Observational

To evaluate the patients' satisfaction with Angeliq Micro in real clinical practice after 13 cycles of treatment.

NCT ID: NCT03118908 Completed - Menopause Clinical Trials

Clinical Evaluation of Effectiveness and Safety of Amberen and Smart B by Women With Climacteric Syndrome

Start date: April 24, 2017
Phase: N/A
Study type: Interventional

To evaluate effectiveness and safety of combined use of dietary supplements Amberen and Smart B by women with a typical (without complications) form of climacteric syndrome, with mild to moderate symptoms.

NCT ID: NCT03112226 Completed - Clinical trials for Cognitive Impairment

Effects of Ovarian Hormone Suppression on Vascular and Cognitive Function

Start date: February 7, 2018
Phase: N/A
Study type: Interventional

Complaints about memory and thinking are common in women as they go through menopause. The female hormone estrogen is important for both the health of both the brain and the blood vessels. In Alzheimer's disease there is damage to the blood vessels in the brain. This study will look at how the loss of the female hormone estrogen affects brain function and the health of blood vessels.