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Female Sexual Dysfunction clinical trials

View clinical trials related to Female Sexual Dysfunction.

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NCT ID: NCT06060691 Completed - Clinical trials for Female Sexual Dysfunction

the Ameliorating Effects of Antioxidant Gel on Female Arousal Disorder and Sexual Dysfunction

Start date: September 20, 2023
Phase: Phase 1
Study type: Interventional

The aim of this study is to evaluate the quality of sexual life of females with sexual interest or arousal disorder before and after accurate application of a formulated emulgel made from natural ingredients, including kaempferol as an API

NCT ID: NCT05833685 Completed - Clinical trials for Female Sexual Dysfunction

Predicting Changes in Core Muscles During Female Sexual Dysfunction: A Comprehensive Analysis Using Machine and Deep Learning

Start date: February 1, 2023
Phase:
Study type: Observational

The purpose of this study is to Predicting changes in core muscles during female sexual dysfunction by A Comprehensive Analysis Using Machine and Deep Learning Female sexual dysfunction (FSD) is a common condition that affects womenof all ages. It is characterized by a range of symptoms, including decreased libido, difficulty achieving orgasm, and pain during intercourse. One potential cause of FSD is muscular weakness or changes in the core muscles. These muscles play an important role in sexual function, and changes in their strength or activation patterns can lead to FSD. Additionally, the development of a machine learning model for this purpose could pave the way for future studies exploring the use of artificial intelligence in the diagnosis and treatment of other musculoskeletal disorder and female health issues.

NCT ID: NCT05806424 Completed - Clinical trials for Female Sexual Dysfunction

Investigation of Awareness Levels of Women Living in Turkey About Kegel Exercises and Pelvic Floor Muscles

Start date: September 21, 2023
Phase:
Study type: Observational

Pelvic floor disorders affect millions of women and their lives in our country and around the world. Along with many factors such as age, obesity, menopause, smoking, number of births and mode of delivery, there is an increase in the prevalence of pelvic floor disorders. Pelvic floor disorders (urinary/fecal incontinence, pelvic organ prolapse, chronic pelvic pain, sexual dysfunction) negatively affect women, their families, caregivers of individuals who cannot meet their own needs, and society in many ways. Treatment of pelvic floor disorders is very costly on a community basis. An effective process is carried out with the use of non-pharmacological traditional and complementary therapies instead of invasive or pharmacological treatment in the early period of the treatment of symptoms of pelvic floor disorders.

NCT ID: NCT04824820 Completed - Clinical trials for Urinary Incontinence

Improving Female Sexual Wellness

Start date: April 10, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effect of commercially available genital vibrator use on sexual health, female pelvic floor disorders, and overall quality of life among a diverse population of women.

NCT ID: NCT04484753 Completed - Clinical trials for Urinary Incontinence

Validation of iPelvis App for Female Pelvic Floor Dysfunction

Start date: January 9, 2017
Phase: N/A
Study type: Interventional

The iPelvis app aims to improve adherence to pelvic physiotherapy on women with pelvic floor related dysfunctions, such as urinary or fecal incontinence, sexual dysfunction, etc.

NCT ID: NCT04384172 Completed - Clinical trials for Spinal Cord Injuries

Effect of Peripheral Neuromodulation on Vaginal Blood Flow

Start date: November 11, 2020
Phase: N/A
Study type: Interventional

The researchers want to see if nerve stimulation interventions cause a change in vaginal blood flow. The effect of this intervention will be compared between women who have neurogenic (spinal cord injury) or non-neurogenic dysfunction and healthy women.

NCT ID: NCT04124640 Completed - Clinical trials for Female Sexual Dysfunction

Observational Study in Real Life to Describe the Libicare® Effectiveness in Female Sexual Dysfunction.

LIBIDOBS
Start date: October 29, 2019
Phase:
Study type: Observational

The decrease or absence sexual desire and arousal is the alteration of the sexual sphere that women most commonly refer to in adulthood and old age. Many women can refer a decrease or absence of desire and / or arousal without having the disorder typified in the DSM-5, but that can cause discomfort, worry and relationship problems in their day to day. Libicare® is a food supplement whose ingredients could have positive effects on the improvement of sexual function in women with low desire and arousal levels. The main ingredients of Libicare® are: - Trigonella Foenum-graecum (Trigonella) (1) - Tribulus Terrestris (Tribulus) (2) - Turnera Diffusa (Damiana) (3)

NCT ID: NCT04122703 Completed - Clinical trials for Female Sexual Dysfunction

Trial of Tibial Nerve Stimulation for Treating Sexual Dysfunction

Start date: September 15, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to understand the efficacy of PTNS versus a placebo in the treatment of female sexual dysfunction syndrome.

NCT ID: NCT03500146 Completed - Overactive Bladder Clinical Trials

Sexual Function Trial of Overactive Bladder: Medication Versus PTNS

STOMP
Start date: January 30, 2017
Phase:
Study type: Observational

Sexual dysfunction affects approximately 45% of women with an even greater incidence reported in women with overactive bladder symptoms, despite this there is a lack of FDA approved treatments for sexual dysfunction in this population. While both medical therapy and electrical neuromodulation have been shown to improve urinary function as well as sexual function, there is a dearth of literature about their comparative effectiveness in the latter. The purpose of this study is to examine the comparative effectiveness of neuromodulation via percutaneous tibial nerve stimulation (PTNS) and medical therapy with anticholinergics or beta-agonists in improving female sexual function. This will be a prospective multi-center cohort study comparing improvement in sexual function as measured by the female sexual function index (FSFI). It is hypothesized that PTNS will improve sexual function to a greater degree than medical therapy as there may be mechanisms by which PTNS directly affects sexual function. Enhanced understanding of the effects of neuromodulation and medical therapy on sexual function may allow for improved patient selection and better outcomes which may lead to widespread use of neuromodulation for female sexual dysfunction.

NCT ID: NCT03479229 Completed - Clinical trials for Female Sexual Dysfunction

Viveve Geneveve Treatment of the Vaginal Introitus to Evaluate Safety and Efficacy

VIVEVE II
Start date: April 20, 2018
Phase: N/A
Study type: Interventional

This study is evaluating the safety and efficacy of the Geneveve Treatment for women experiencing diminished sexual function following vaginal childbirth. Participants will be randomized to either active or sham treatment and followed for 12 months.