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Sexual Dysfunction clinical trials

View clinical trials related to Sexual Dysfunction.

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NCT ID: NCT04764578 Withdrawn - Sexual Dysfunction Clinical Trials

Sexual Dysfunction Following Upper Extremity Trauma

Start date: March 1, 2022
Phase:
Study type: Observational

Hypothesis 1. The prevalence of sexual dysfunction after upper extremity function in adults (>18yo) is higher than the general population in the early post-operative period (3mo) and at 1 year post-operatively. 2. Null: Adult patients (<18 yo) with isolated upper extremity trauma do not experience sexual dysfunction more than the general population. Primary Study Question a) What is the prevalence of sexual dysfunction after upper extremity trauma (fracture, soft tissue disruption, neurovascular injury, and completion amputation) in adult patients? Secondary Study Questions 1. Are there patient or injury factors that can predict sexual dysfunction? 2. Do certain fractures cause more sexual dysfunction than others? 3. Can we accurately predict which patients may experience sexual dysfunction post-injury?

NCT ID: NCT04716738 Not yet recruiting - Clinical trials for Irritable Bowel Syndrome

Visceral Sensitivity in Women With BS and Sexual Dysfunction

IBS
Start date: February 1, 2023
Phase:
Study type: Observational [Patient Registry]

This study aims to compare visceral rectal sensitivity and quality of life of 40 Irritable Bowel Syndrome women, with (20) and without sexual dysfunction (20). Both Irritable Bowel Syndrome (IBS) and sexual dysfunction (SD), decrease quality of life (QOL) separately, and only recently we have shown that quality of life decreases even more with both diseases. Thus, there is clinical evidence to search for a biological marker that explains this cumulative effect. Investigators will determine IBS using the Rome IV criteria, SD through the Female Sexual Function Index (FSFI) while and QOL through the Short Form-36 and the IBS-QOL. Visceral sensitivity will be evaluated by a barostat study: A small bag connected to a computer is placed in the rectum. This computer will insufflate air increasing the volume and simultaneously record the pressure inside the rectum; therefore investigators can simulate what happens when the stool reaches the rectum. The patient reports the first sensation, gas sensation, need to defecate and even pain. For patient protection the pressure will never exceed 50 mmHg and/or if any amount of pain is reported. To assess the effect of food on this visceral sensitivity, it is performed in 2 stages, fasting and 30 minutes after a standardized meal. The protocol will be carried out through 3 visits. First patients will be recruited; the diagnosis of IBS, SD, quality of life will be established and basic laboratory tests will be schedule before next visit. Second visit will be on day 7 of the menstrual cycle when investigators will carry out the barostat study and determination of blood´s sex hormones. The last visit is for the second barostat study on day 21 of the menstrual cycle with sex hormones measurement. This protocol will compare: Rectal pressure and volume for tone, first sensation, gas sensation, desire to defecate and pain, measure during fasting and postprandial periods in day 7 and 21 (estrogenic and progesterone phase) of the menstrual cycle. Other variables include (age, marital status, disease history, SF-36, IBS-QOL, etc.). This study aims to find a biological marker to explain the low QOL observed in daily clinical practice. This approach will allow us a more effective diagnosis and perhaps the creation of more effective therapeutic approaches to treat these patients. In the long term, we expect to establish the foundations of a patient-centered medicine with shared decision more effective in the gut brain axis disorders.

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: NCT04684602 Recruiting - Autoimmune Diseases Clinical Trials

Mesenchymal Stem Cells for the Treatment of Various Chronic and Acute Conditions

Start date: July 9, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

This multi-arm, multi-site study investigates the safety, tolerability, and efficacy of stem cell therapy for the treatment of various acute and chronic conditions. Clinically observed initial findings and an extensive body of research indicate regenerative treatments are both safe and effective for the treatment of multiple conditions.

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: NCT04544735 Suspended - Gynecologic Cancer Clinical Trials

Improving Women's Function After Pelvic Radiation

Start date: October 7, 2020
Phase: N/A
Study type: Interventional

The purpose of the study is to develop and test an intervention combining physical therapy (PT) and coping skills training to improve women's sexual function after pelvic radiation.

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: NCT04411485 Recruiting - Clinical trials for Ankylosing Spondylitis

Sexual Dysfunction in Partner of Patients With Ankylosing Spondylitis

Start date: February 15, 2018
Phase:
Study type: Observational

The adverse effects of rheumatologic diseases, especially Ankylosing Spondylitis (AS), on sexual functions are known. The causes of sexual dysfunction in rheumatologic diseases are due to factors such as pain, weakness, fatigue, stiffness, functional disability, anxiety, depression, hormonal deficiency, drug use, decreased libido and poor body image. Depending on these factors, sexual intercourse and frequency of sexual intercourse may decrease. Sexual dysfunction may be seen in AS due to physical and emotional problems caused by the disease.