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Sexual Dysfunction clinical trials

View clinical trials related to Sexual Dysfunction.

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NCT ID: NCT04708249 Completed - Sexual Dysfunction Clinical Trials

D-chiroinositol Administration in Hypogonadal Males

Start date: January 18, 2021
Phase: N/A
Study type: Interventional

D-chiroinositol (DCI), is known as second messenger of insulin pathway, but recently several works have reported the influence of DCI on steroidogenesis. In particular, the DCI capabilities to regulate aromatase expression and testosterone biosynthesis are arising. In this regard, DCI administration in case of reduced levels of testosterone, could be a good therapeutic opportunity. For this reason, the treatment of Late-Onset Male Hypogonadism (LOH) in undoubtedly an interesting target. LOH is a reduction of testosterone level due to advancing age, currently treated with Testosterone Replacement Therapy (TRT). Unfortunately, there is a lack of information about TRT safety, especially in older men. For these reasons, the aim of this study is to evaluate the effect of DCI treatment on testosterone accumulation in LOH patient.

NCT ID: NCT04662398 Completed - Clinical trials for Erectile Dysfunction

Using of Testes' Shocker in Improving Sexual Activity

Start date: December 5, 2020
Phase: N/A
Study type: Interventional

Using of testes' shocker in treating the sexual dysfunction.

NCT ID: NCT04560283 Completed - Sexual Dysfunction Clinical Trials

HYDEAL-D® Application for Promoting the Restoration of Sexual Function in the Postpartum Period

HYDEAL-D
Start date: September 1, 2016
Phase: Phase 4
Study type: Interventional

During postpartum and lactation, vaginal epithelium tends to have an impaired degree of hydration and lubrication. This may lead to vaginal dryness, burning sensation dyspareunia or itching, which negatively affect the sexual function of puerperal women. This study aimed to evaluate the efficacy of HYDEAL-D® vaginal gel (HYALOGYN®, Fidia Farmaceutici, Abano Terme, Italy) application on promoting the restoration of sexual function in the postpartum period.

NCT ID: NCT04472104 Completed - Sexual Dysfunction Clinical Trials

BREast Cancer And Sexuality Treatment

BREAST
Start date: January 6, 2020
Phase: N/A
Study type: Interventional

The purpose of this project is to compare the effects of a group mindfulness treatment versus a group sex education on sexual desire, sexual distress, and sexual pain in breast cancer (BrCa) survivors. Participants will be randomly assigned to either 8 weekly sessions of a group mindfulness-based treatment or 8 weekly sessions of a sex education group. Groups will consist of approximately 8 breast cancer survivors and will be led by 2 trained therapists. Participants will complete four assessments (involving a clinician administered interview and standardized questions): pre-treatment, post- treatment, and 6 month follow up.

NCT ID: NCT04415710 Completed - Clinical trials for Urinary Incontinence

Pelvic Floor and Sexual Dysfunction in Women With Sjogren's Syndrome

Start date: February 21, 2019
Phase:
Study type: Observational [Patient Registry]

Sjogren's syndrome (SS) is a chronic, systemic, autoimmune disease characterized by lymphocytic infiltration of all exocrine glands, especially tear and salivary glands, and is more common in women.

NCT ID: NCT04395885 Completed - Sexual Dysfunction Clinical Trials

Sexual Function During COVID 19 Pandemic

Start date: June 1, 2020
Phase:
Study type: Observational

The outbreak of a new Coronavirus disease (COVID-19), caused by the 2019-nCoV infection in December 2019 is one of the most severe global epidemic health problems.The rapid contagion of this Novel virus has provoked the World Health Organization (WHO) to classifying the outbreak as a "Public Health Emergency of International Concern" on January 30 2020 to a "Pandemic" on March 11th 2020

NCT ID: NCT04378478 Completed - Sexual Dysfunction Clinical Trials

Urological Management of Complications of Penile Constriction Devices:

PCD
Start date: July 1, 2020
Phase:
Study type: Observational

Wearing a penile ring is justified by international societies of Urology (AFU, EAU, AUA) only for the treatment of erectile dysfunction with vacuum. In this case, it is a constriction rubber band that can only be worn for 30 minutes. Nowadays, wearing a cockring device for recreational purposes can lead to complications secondary to ischemia caused by strangulation of the penis and/or scrotum. The variety of devices and materials used (metallic and/or alloys in particular) sometimes makes it difficult to remove them, requiring expensive surgery and dedicated equipment. There is no official recommendation for the management of these complications.

NCT ID: NCT04287205 Completed - Endometriosis Clinical Trials

The Effect of Dydrogesterone on Sexual Function in Women With Endometriosis

Start date: April 20, 2019
Phase: N/A
Study type: Interventional

This study aimed to assess the effects of dydrogesterone on sexual function in women with endometriosis using Female Function Sexual Index (FSFI).

NCT ID: NCT04228679 Completed - Sexual Dysfunction Clinical Trials

Erbium Laser for Treatment of Vaginal Looseness and Sexual Dysfunction.

Start date: April 1, 2020
Phase: N/A
Study type: Interventional

Patients with a primary complaint of vaginal looseness and sexual dysfunction, visiting a sexual dysfunction clinic at a tertiary medical center will undergo randomization to either a series of 3 laser treatments or 3 sham treatments, and the effect of these treatments will be measured by several validated questionaires and by means of gynecological examination.

NCT ID: NCT04221607 Completed - Breast Cancer Clinical Trials

An Intimacy Intervention for Couples Completing Breast or Prostate Cancer

Start date: December 9, 2019
Phase: N/A
Study type: Interventional

This project seeks to help patients address and improve intimacy at the end of treatment for breast or prostate cancer. It is intended to address the needs of cancer survivors, broadly defined as paftients and their loved ones or caregivers facing a cancer diagnosis. While we know sexual health is impacted by the diagnosis and treatments for cancer, we also are increasingly aware that partners and spouses are also impacted by the experience. Yet, there are no evidence based interventions that focus on the couple's recovery after the initial cancer experience. The objective of this study is to look at the impact of an intimacy intervention at the completion of cancer treatment for couples facing breast or prostate cancer. We will enroll patients and their intimate partners in this study in two phases. In the first phase, couples will receive sensate focus homework, explained to them at a standard survivorship care visit (SCV) by a study nurse practitioner (NP). The objective in the first phase is to see if this is something feasible by looking at how many use sensate focus homework in 6 weeks. If it is not feasible, we will rework the study based on what we learned. However, if it is feasible, we will reopen the study to a larger group and employ a random assignment to an SCV with or without sensate focus homework. This phase will give us evidence of efficacy that we will use to propose a larger randomized trial, potentially in the National Cancer Institute system. Participants will be asked to answer questionnaires at baseline, 6 weeks, and then at 12 weeks during phase 2. Those who complete treatment at 12 weeks will be re-contacted 6 months after protocol enrollment for an optional end of treatment interview to assess what they thought of the intervention, including sensate focus homework itself and the timing.