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Female Sexual Dysfunction clinical trials

View clinical trials related to Female Sexual Dysfunction.

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NCT ID: NCT06060691 Recruiting - 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: NCT05337813 Recruiting - Overactive Bladder Clinical Trials

Effects of Low-intensity Excoporeal Shock Wave Therapy (LiESWT) on Women With Pelvic Floor Dysfunction

Start date: April 10, 2020
Phase: N/A
Study type: Interventional

1. This study needles female reproductive urinary tract, likely bladder hyperactivity, active urinary incontinence and interstitial cystitis, observation use of low-capacity seismic wave (LiESWT) therapy combined with combined platelet plasma (PRP), improved bone basin pain and female Urinary incontinence. 2. LiESWT to arousal the clitoris angiogenesis to prevent female sexual dysfunction.

NCT ID: NCT04885556 Recruiting - Dyspareunia Clinical Trials

Evaluation of a Novel Female Hygiene Device for Postcoital Discomfort

Start date: April 5, 2021
Phase: N/A
Study type: Interventional

Previous research has shown that semen deposition in the vagina after intercourse leads to dripping, discomfort, and vaginal odor. This study is evaluating a hygiene device designed to be inserted into the vagina after intercourse to absorb semen deposited into the vaginal canal to determine if there is a reduction in dripping and odor, and to determine the amount of fluids absorbed.

NCT ID: NCT04419961 Recruiting - Clinical trials for Female Sexual Dysfunction

Sexual Dysfunction and an Educational Program to Improve the Quality of Sexual Function in Vietnamese Pregnant Women in First Trimester

Start date: September 15, 2020
Phase: N/A
Study type: Interventional

Sexual dysfunction is common in pregnant women (46.6%, 34.4%, and 73.3% in women in the first, second, and third trimester worldwide, respectively). These dysfunctions can persist after childbirth, affecting quality of life, marriage satisfaction, and family happiness. In Vietnam, a country heavily influenced by the Eastern traditions, sexual activity is considered private and only shared between husband and wife. Many women have wrong beliefs that having sexual intercouse during pregnancy will affect the safety of the fetus, and thus, are reluctant to engage in sexual activity with their husband. Interventions have been developed to improve the quality of sexual function in pregnant women. In Vietnam, data of sexual dysfunction in pregnant women are somewhat limited, and there have been no programs to improve the sexual function for this population. Therefore, the study team plans to develop an educational program with aim to improve the quality of sexual function in Vietnamese pregnant women. This study aims to investigate the prevalence and associated factors of sexual dysfunction in first-trimester pregnant women and evaluate the effectiveness of the educational program.

NCT ID: NCT04384172 Recruiting - 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: NCT03498443 Recruiting - Clinical trials for Female Sexual Dysfunction

Effect of Pelvic Organ Prolapse Surgeries on Female Sexual Function in Egyptian Women

Start date: September 1, 2017
Phase:
Study type: Observational

study on female sexual function after different prolapse surgeries

NCT ID: NCT01078077 Recruiting - Clinical trials for Female Sexual Dysfunction

The Impact of a Topical Vasodilating Cream on Female Sexual Experience

TVConFSD
Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine if a topical vasodilating cream will improve female sexual experience.

NCT ID: NCT00142714 Recruiting - Multiple Sclerosis Clinical Trials

Effects of Spinal Cord Injury on Female Sexual Response

Start date: August 2003
Phase: N/A
Study type: Interventional

The long term aims of this project are to 1) Understand the effect of varying degrees and levels of SCI and dysfunction(SCI/D)on females sexual response: 2) Identify the specific neuronal pathways involved in female sexual responses; and 3) Develop and evaluate new assessment and treatment methods for neurogenic sexual dysfunction in women.