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Menopause Related Conditions clinical trials

View clinical trials related to Menopause Related Conditions.

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NCT ID: NCT06318403 Not yet recruiting - Menopause Clinical Trials

Estradiol Supplementation and Rotator Cuff Repair

ESTRCR
Start date: April 2025
Phase: Phase 2
Study type: Interventional

Rotator cuff tears in the shoulder are common, often cause pain and disability, often fail to heal with surgery, and both tears and failure of healing are associated with estradiol deficiency. In this study, women who have gone through menopause will be randomized to either estradiol patches or placebo patches after repair of the rotator cuff. The purpose of this study is to determine whether estradiol patches show promise in improving shoulder pain, strength, and function when given with rotator cuff repair.

NCT ID: NCT06176820 Not yet recruiting - Sexual Dysfunction Clinical Trials

Vaginal Hyaluronic Acid, Arginine and Liposome Gel Versus Vaginal Lubricant in Postmenopausal Women With Genitourinary Syndrome of Menopause

VHAL
Start date: January 1, 2024
Phase: Phase 2/Phase 3
Study type: Interventional

The goal of this interventional study is to compare the efficacy and safety of vaginal hyaluronic acid, arginine and liposome gel versus vaginal lubricant in the treatment of genitourinary syndrome of menopause in postmenopausal women. The main question it aims to answer is: Is vaginal hyaluronic acid, arginine and liposome gel more effective than vaginal lubricant in the treatment of genitourinary syndrome of menopause in postmenopausal women Participants will be randomized into 2 treatment groups: vaginal hyaluronic acid, arginine and liposome group and vaginal lubricant group. Researchers will compare whether vaginal hyaluronic acid, arginine and liposome group has better improvement than vaginal lubricant group.

NCT ID: NCT04190927 Not yet recruiting - Menopause Clinical Trials

A New Hormone Replacement Paradigm: Physiologic Restoration Study

Start date: June 1, 2020
Phase: Phase 4
Study type: Interventional

This is a three-year, prospective, observational study looking at the benefits of rhythmically dosed, bio-identical hormones compounded in a carrier cream in 100 symptomatic peri and postmenopausal women. This study will measure changes in cognition, mood, quality of life, endocrine health, bone mineral density, and reduction of the symptoms of menopause and any adverse effects. The objectives of this study are to show that rhythmic dosing of bio-identical hormones that mimic a menstrual cycle, are possible, and may be more beneficial and have fewer side effects than the current standard of care for treating the symptoms of menopause.