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Menopause clinical trials

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NCT ID: NCT01816360 Completed - Menopause Clinical Trials

Aromatherapy and Yogatherapy for Hot Flashes

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to verify and analyse psychological and physiological effects of olfactory aromatherapy and yogatherapy respiratory exercises, together and separately, on the quality of life, levels of stress, quality of sleep and intensity and frequence of hot flashes in climacteric women.

NCT ID: NCT01805765 Completed - Menopause Clinical Trials

Qing'E Formula Therapy on Menopausal Symptoms

Start date: March 2013
Phase: Phase 2/Phase 3
Study type: Interventional

The objective of this study is to evaluate whether a Chinese medicine formula (Qing'E) is effective in alleviating menopausal symptoms and safety.

NCT ID: NCT01805674 Completed - Menopause Clinical Trials

Isoflavones and Magnolia Extract in the Quality of Life in Menopausal Women

ESTROCALVI
Start date: March 2013
Phase: N/A
Study type: Observational

In menopause, the vasomotor symptomatology, accompanied or less by affective and behavioural symptoms, globally worsens the quality of daily life. The improvement of the quality could be reached with adequate food supplements, named phytoestrogens, in particular Soy Isoflavones (SI), which are natural substances with estrogen-like and estrogen-antagonistic activity, which are active in the control of menopausal vasomotor symptoms. Besides, combined with magnolia extract it could improve the psychological symptomatology also improving the quality of life.

NCT ID: NCT01778985 Completed - Menopause Clinical Trials

Effect of Preoperative Estrogen Treatment on Connective Tissues of the Pelvic Floor

PET
Start date: December 2012
Phase: Phase 4
Study type: Interventional

This is a study to determine how vaginal estrogen cream given for several weeks before pelvic reconstructive therapy will effect elastic fiber assembly in the muscularis layer of the vaginal wall. Postmenopausal women with at least Stage 2 pelvic organ prolapse will receive either estrogen vaginal cream or placebo cream 6-8 weeks prior to reconstructive surgery. At time of surgery, full thickness biopsies will be obtained from a standardized location at the top of vagina. The investigators will measure the thickness of the vaginal muscularis, elastic fiber number and morphology, and analyze if elastic fiber synthesis or degradation is affected by estrogen therapy. The results will provide important data to support a larger clinical trial to determine if preoperative and maintenance estrogen therapy alter long-term success rates of pelvic reconstructive surgery for pelvic organ prolapse.

NCT ID: NCT01778712 Completed - Obesity Clinical Trials

Developing an Intervention to Prevent Visceral Adipose Tissue Accumulation

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

The aim of this study is to develop an intervention that will produce a sustained improvement in physical activity and chronic stress as a means to slow the menopause-related accumulation of visceral adipose tissue in mid-life women.

NCT ID: NCT01757340 Completed - Obesity Clinical Trials

Calorie Restriction With Leucine Supplementation

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

The purpose of this study is to determine whether consuming additional leucine during calorie restriction induced weight loss has beneficial or harmful effects on multi-organ (liver, muscle, adipose tissue) insulin sensitivity, colonocyte proliferation rates, the gut microbiome, muscle mass and function, and bone mineral density in obese, postmenopausal women.

NCT ID: NCT01705249 Completed - Healthy Clinical Trials

Bleeding Profile With Continuous Hormone Replacement Therapy of Activelle® in Postmenopausal Women

Start date: August 14, 2001
Phase: Phase 4
Study type: Interventional

This study is conducted in Europe. The aim of this study is to investigate the bleeding profile after switch from Trisekvens® to Activelle® (1.0 mg estradiol / 0.5 mg norethisterone acetate (NETA)).

NCT ID: NCT01679899 Completed - Clinical trials for Type 2 Diabetes Mellitus

Effect of Anti-diabetic Drugs on Bone Metabolism and Glycemic Variability

BoneGlyc
Start date: December 2012
Phase: Phase 4
Study type: Interventional

This is a Monocentric, Prospective, Randomized, Open-label, Comparative, Phase IV Study, to compare the effects of Vildagliptin and Gliclazide MR on Markers of Bone Remodeling, Bone Mineral Density and Glycemic Variability in Postmenopausal Women with Type 2 Diabetes. A total of 38 women with documented Type 2 Diabetes and menopause will be enrolled. The active treatment will include a 50 mg dose of vildagliptin OD twice a day. As comparator, gliclazide MR will be administered at a dose of 60 to 120 mg OD once a day.

NCT ID: NCT01596010 Completed - Healthy Clinical Trials

Investigation of 2 Different Oral Formulations of Estradiol and Norethisterone in Healthy Women

Start date: October 2007
Phase: Phase 1
Study type: Interventional

This trial is conducted in Europe. The aim of this trial is to investigate whether a reformulated estradiol/norethisterone acetate (NETA) formulation is bioequivalent to that of Kliogest® (estradiol/norethisterone acetate (NETA) in healthy women.

NCT ID: NCT01543399 Completed - Menopause Clinical Trials

Vascular Effect of Tibolone in the Brachial Artery

TDILA
Start date: March 2012
Phase: N/A
Study type: Interventional

The interruption of the secretion of sex steroids occurring during menopause, causes a change in vascular pattern at various levels. As a result, several agencies have side effects that interfere with women's health. The use of hormone replacement therapy has contributed to the improvement in these effects. In previous studies the investigators showed the effect of sex steroids in premenopausal women in the conjugated equine estrogens, medroxyprogesterone acetate and tibolone in menopausal women, on the central retinal arteries. The aim of this study is to evaluate the effects of Tibolone in Flow-Mediated Dilatation of the brachial artery.