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Sexual Dysfunction clinical trials

View clinical trials related to Sexual Dysfunction.

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NCT ID: NCT05856929 Recruiting - Sexual Dysfunction Clinical Trials

Sexual Dysfunction After Renal Transplantation

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

A questionnaire will be send to kidney transplant recipients to investigate characteristics of them and their sexual function, all participants in the survey are anonymous and voluntary, then analyse these characteristics.

NCT ID: NCT05837117 Active, not recruiting - Sexual Dysfunction Clinical Trials

Sexual Dysfunction in Palliative Care Patients: An Assessment of Patient's Perspective

Start date: December 15, 2022
Phase:
Study type: Observational

To learn about the communications that Supportive Care patients receive about sexual well-being from their healthcare provider. Researchers also want to learn about your attitudes, beliefs, and feelings about sexual well-being.

NCT ID: NCT05836675 Not yet recruiting - Clinical trials for Chronic Kidney Diseases

Quality of Life and Sexual Life in Hemodialysis Patients: Effects of an Intradialytic Exercise Program

Start date: May 2023
Phase: N/A
Study type: Interventional

The aim of the study is to investigate whether an intradialytic exercise program can improve the quality of life, sexual function, and sexual satisfaction in patients undergoing hemodialysis.

NCT ID: NCT05832268 Enrolling by invitation - Clinical trials for Urinary Incontinence

Pelvic Floor Function After Obstetric Injury to the Anal Sphincter

PFF
Start date: September 19, 2023
Phase:
Study type: Observational [Patient Registry]

The goal of this observational study is to learn more about the effect a pregnancy and delivery has on the function of the anal musculature.We will compare women who had a new delivery after suffering a severe tear in the anal musculature in their first pregnancy, with women who had two or more vaginal deliveries, but did not suffer such an injury. The main questions we want to answer is: - can the burden of a new pregnancy and delivery weaken the function of the repaired musculature in a way that might cause symptoms of anal incontinence later in life? - can a tear in the anal musculature increase the risk of developing urinary incontinence and long term sexual dysfunction? - should we recommend these women to have a caesarian section instead of a new vaginal delivery? Participants will be asked to complete an electronic questionnaire with information regarding their pregnancies, deliveries and potential symptoms from anal incontinence, urinary incontinence and sexual dysfunction. Researchers will compare these two groups to find out if a new vaginal delivery has a negative effect on the function of the anal musculature.

NCT ID: NCT05826691 Recruiting - Quality of Life Clinical Trials

Benign Prostate Surgery and QOL and Sexual Function

BEPS
Start date: September 1, 2021
Phase:
Study type: Observational [Patient Registry]

Rationale: A variety of surgical techniques have been described for surgical treatment of male LUTS because of BPH, which has different outcomes and may result in adverse events regarding ejaculatory function and erection, resulting in a negative impact on QOL on short- and mid-term follow-ups. Objective: To compare outcomes of BPH surgery using a conventional versus ejaculation preserving technique on QOL-related aspects with emphasis on ejaculatory and erectile function. Study design: This study is a prospective longitudinal multi-center trial to compare the ejaculatory and erectile function outcomes between conventional and ejaculation preserving BPH surgical procedures/techniques. Baseline characteristics will be recorded, as well as short and mid-term follow-up. Study population: The study population comprises patients who will undergo BPH surgery in the participating centers. Intervention: All patients will undergo BPH surgery (including but not restricted to Monopolar / Bipolar Transurethral resection of the prostate (TURP), photo vaporisation (PVP), Plasmakinetic (PK), Holmium laser enucleation of the prostate (HOLEP) or open prostatectomy (OP)). Main study parameters/endpoints: Primary endpoint is to compare the baseline to the short-term (3 months) and mid-term (6 months) ejaculation function and QoL outcomes. The secondary endpoint is the short and mid-term erection function and QoL outcomes compared to baseline. Nature and extent of the burden and risks associated with participation, benefit, and group relatedness: Patients' burden and risk associated with participating in this trial do not differ among surgical procedures or techniques used. In all groups, patients will undergo a BPH surgery and will be followed for six months at 3 visits.

NCT ID: NCT05805228 Completed - Pregnancy Related Clinical Trials

Sexual Life of Couples During Pregnancy and Postpartum Period

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

The aim of this clinical trials is to determine the effect of sexual counseling applied in line with a special counseling model on the sexual functions of couples during pregnancy and postpartum period in order to prevent sexual problems that may occur in the pregnant woman and her husband during pregnancy. The main questions it aims to answer are: 1. Does sexual counseling to be conducted during pregnancy prevent the problems that may occur in women during pregnancy and postpartum period? 2. Does sexual counseling to be conducted during pregnancy prevent the problems that may occur in pregnant women's husband during pregnancy and postpartum period? Questionnaires evaluating the sexual lives of the participants were administered. Afterwards, sexual counseling was given to the pregnant woman and her husband in the first three months of pregnancy. After the counseling, the questionnaires were applied again in the later stages of pregnancy and in the postpartum period. In order to see whether sexual counseling affects sexual problems that may develop during pregnancy and postpartum period, the researchers compared the counseling couples with the pregnant women who did not receive counseling and their spouses.

NCT ID: NCT05761275 Not yet recruiting - Quality of Life Clinical Trials

Assessment of Women's Sexual Quality of Life After Benign Adnexal Surgery Using vNOTES Approach

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

Transvaginal Natural Orifice Transluminal Endoscopic Surgery (vNOTES) is a recent innovation in minimally invasive surgery which has already proven its non-inferiority to conventional abdominal laparoscopy (CAL) for hysterectomy in terms of efficiency and safety. However, the investigators note a lack of medical literature and no specific randomized controlled trial (RCT) assessing women's sexual function after vNOTES for benign adnexal surgery. The aim of this RCT is to confirm the non-inferiority of the vNOTES approach for benign adnexal pathology compared to CAL on women's sexual function. Secondary outcomes will evaluate vNOTES's efficiency, morbidity and postoperative complications compared to CAL for benign adnexal surgery. The relationship between adnexal mass morcellation/aspiration and the quality of the histological analysis on surgical specimens will also be evaluated as secondary outcome.

NCT ID: NCT05749471 Recruiting - Sexual Dysfunction Clinical Trials

Sex Dysfunction and Chronic Venous Disease

SEXVENO
Start date: January 1, 2019
Phase:
Study type: Observational

Chronic Venous Disease (CVD) is a common clinical condition with a high prevalence in the western population that may affect quality of life (QoL) of affected patients for several adverse effects. Sexual dysfunction (SD) also partecipate in the QoL of people and has never specifically studied in CVD patients. The aim of this study is to study SD in CVD patients before and after treatment.

NCT ID: NCT05732844 Completed - Clinical trials for Urinary Incontinence

Efficacy of the Use of Vaginal Balls for the Improvement of Urinary Incontinence and Sexual Function in Women.

Start date: October 5, 2022
Phase: N/A
Study type: Interventional

Asess if adding vaginal spheres treatment to the conventional Pelvic Floor Muscle Trainning (PFMT) produces a greater decrease in the severity of the stress urinary incontinence or a greater perceived quality of life related to incontinence.

NCT ID: NCT05727566 Recruiting - Sexual Dysfunction Clinical Trials

Sexual Dysfunction in Patients With Myofascial Pain Syndrome

Start date: May 11, 2022
Phase:
Study type: Observational

This study evaluates the frequency of sexual dysfunction in women with myofascial pain syndrome and its relationship with clinical parameters.