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Ejaculatory Dysfunction clinical trials

View clinical trials related to Ejaculatory Dysfunction.

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NCT ID: NCT05914519 Not yet recruiting - BPH Clinical Trials

Outcomes and Efficacy of Ejaculatory Preserving Transurethral Resection of Prostate

Start date: July 1, 2023
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the outcomes and efficacy of ejaculatory preserving TURP in terms of voiding, erectile function, and ejaculation.

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: NCT05650853 Completed - Clinical trials for Ejaculatory Dysfunction

Exploration of eJaculatory Anatomy Concept Study (EJAC Study)

Start date: December 12, 2022
Phase: N/A
Study type: Interventional

Ejaculatory dysfunctions (ED) are an important cause of postoperative dissatisfaction, which lead to a decrease in the intensity of orgasms in 50% of patients. ED is a cause for concern for almost a third of patients who need surgery. Surgical techniques have been developed to limit the occurrence of postoperative ED, but their results remain heterogeneous. There are very few studies on the biomechanical anatomy of ejaculation. Ejaculation is a complex phenomenon involving different structures and in particular the Veru Montanum. This is the key element in the emission of ejaculate within the prostatic urethra. In addition, there is a structure located in the resection zone of the prostate adenoma. It has therefore been suggested that its resection was a primary source of ED. A single observational study carried out in by Gil Vernet et al in 1994 evaluated on a single healthy 18-year-old volunteer the ejaculatory mechanism of expulsion using an endorectal probe recording the movements of the prostate, the bladder neck and of the proximal urethra during ejaculation. A contemporary study of the biomechanics of the ejaculatory expulsion phase could confirm and improve understanding of the involvement of anatomical structures. The results of our study aim to adapt surgical techniques aimed at limiting the risk of postoperative ED.

NCT ID: NCT05468931 Recruiting - Clinical trials for Erectile Dysfunction

Prostate Stimulation for Sexual Dysfunction

Start date: April 18, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to use a device to stimulate the prostate with a goal of helping improve symptoms in men with sexual dysfunction.

NCT ID: NCT05370651 Recruiting - Clinical trials for Ejaculatory Dysfunction

Emsella Chair vs Sham for Male Sexual Dysfunction

Emsella_EJD
Start date: December 14, 2022
Phase: N/A
Study type: Interventional

We will be performing this study in 2 phases: Phase 1 will be an open label pilot study of 10 male participants. All participants in the pilot study will receive active treatment. If data from the pilot study is suggestive of symptom improvement, we will continue on to phase 2, which is a sham controlled, randomized blinded study. Participants in phase 2 will be randomized to receive either active treatment or sham. Potentially total of 114 participants for both phases will be enrolled. The purpose of this study is to compare the Emsella Chair to sham and to determine whether electromagnetic technology is effective in the treatment of sexual dysfunction, specifically erectile dysfunction (EjD) in men.

NCT ID: NCT04115540 Completed - Delayed Ejaculation Clinical Trials

Penile Nerve Stimulation for Treatment of Delayed Ejaculation

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

The aim of this clinical trial is to test the safety and feasibility of using transcutaneous electrical nerve stimulation (TENS) of the penile nerves to reduce intra-vaginal ejaculatory latency time in men with delayed ejaculation (DE). We hypothesize that this type of stimulation, either before or during sexual activity, will reduce latency time. The primary objective of this study is to determine if TENS of the penile nerve helps men with DE subjectively reduce their ejaculatory latency time. The secondary objective is to determine whether their International Index of Erectile Function (IIEF) score improves with treatment.

NCT ID: NCT03176017 Recruiting - Clinical trials for Prostate Hyperplasia

Ejaculatory Sparing Transurethral Incision Of The Prostate (ES-TUIP) Versus Conventional TUIP

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

In this study, Investigators planned to compare ejaculatory sparing and non-ejaculatory sparing (conventional) TUIP using both subjective and objective assessment tools for the degree of deobstruction. Furthermore, the impact of both techniques on ejaculation and its secondary effect on orgasm perception and different domains of sexual function will be thoroughly assessed.

NCT ID: NCT01419236 Completed - Hypogonadism Clinical Trials

A Study of Ejaculatory Dysfunction in Men With Low Testosterone Levels

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if testosterone solution 2% can impact symptoms of ejaculatory dysfunction in men with low testosterone.