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Erectile Dysfunction clinical trials

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NCT ID: NCT01442077 Recruiting - Clinical trials for Erectile Dysfunction

Low Intensity Extracorporeal Shock Wave Therapy for the Treatment of Erectile Dysfunction- 4 Arms

Start date: November 2011
Phase: Phase 3
Study type: Interventional

Low intensity shock waves(LISW) have been proven in animal studies to induce local growth of new blood vessels. The investigators hypothesized that LISW therapy could improve the symptoms of patients with erectile dysfunction resulting from a problem of blood supply who respond to oral therapy (PDE-5 inhibitors). The current study will check 4 different arm.

NCT ID: NCT01317693 Recruiting - Clinical trials for Erectile Dysfunction

Extracorporeal Shock Wave Therapy With a Wide Focus Probe for the Treatment of Erectile Dysfunction

Start date: March 2011
Phase: Phase 3
Study type: Interventional

Low intensity shockwaves (1/10 the ones used in Lithotripsy) are delivered to the penile tissue. Shockwaves are created by a special generator and are focused using a specially designed shockwave applicator apparatus. The shockwaves are delivered through the applicator covering the corpora cavernosa of the penis. In previous studies the investigators used a medium focused probe and in this study the investigators are evaluating results of this therapy using a wider focus probe in the aim of improving results of treatment.

NCT ID: NCT01317680 Recruiting - Clinical trials for Erectile Dysfunction

Low Intensity Shock Wave Therapy (LI-ESWT) for Erectile Dysfunction in Post Radical Prostatectomy Patients Not Responding to PDE5 Inhibitors (LI-ESWT)

LI-ESWT
Start date: March 2011
Phase: Phase 3
Study type: Interventional

Low intensity shock waves (LISW) have been proven in animal studies to induce local growth of new blood vessels. The investigators hypothesized that LISW therapy could improve the symptoms of patients with erectile dysfunction resulting from a problem of blood supply (damage that can occur after radical prostatectomy in addition to neural damage or solely) that do not respond to oral therapy (PDE-5 inhibitors).

NCT ID: NCT01315262 Recruiting - Clinical trials for Erectile Dysfunction

On Demand Versus Daily Sildenafil for Patients Undergoing Radical Prostatectomy

URO2010
Start date: January 2011
Phase: Phase 3
Study type: Interventional

Viagra (Sildenafil citrate) is an orally active selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) which is used for the treatment of erectile dysfunction (ED). Objectives: - To test the efficacy of Viagra 100mg on demand vs. Viagra 100mg daily (taken either at bedtime or 1 hour prior to sexual intercourse) in restoring erectile function following radical prostatectomy. - To test the safety and tolerability of Viagra 100 mg on demand vs. Viagra 100 mg daily after radical prostatectomy.

NCT ID: NCT01274923 Recruiting - Clinical trials for Erectile Dysfunction

Double Blind Placebo Controlled Study on the Effect of Extracorporal Shock Wave Therapy on Erectile Dysfunction in PDE5i Responders

LI-ESWT
Start date: August 2010
Phase: Phase 3
Study type: Interventional

This study aims to evaluate the effect of shockwave therapy on erectile dysfunction on patients responding to PDE5i therapy in a sham controlled randomized double blind manner.

NCT ID: NCT01262157 Recruiting - Clinical trials for Erectile Dysfunction

Low Intensity ShockWave Therapy for ED in Non Responders to PDE5i - a Double Blind Placebo Controlled Study

LI-ESWT
Start date: April 2010
Phase: Phase 3
Study type: Interventional

Low intensity shock waves (LISW) have been proven in animal studies to induce local growth of new blood vessels. The investigators hypothesized that LISW therapy could improve the symptoms of patients with erectile dysfunction resulting from a problem of blood supply that do not respond to oral therapy (PDE-5 inhibitors).

NCT ID: NCT01249703 Recruiting - Clinical trials for Erectile Dysfunction

The Early Diagnosis and Warning Role of Erectile Dysfunction

Start date: January 2008
Phase: N/A
Study type: Observational

1. Find the early diagnostic markers of erectile dysfunction; 2. Study the warning role of ED in some diseases.

NCT ID: NCT01194648 Recruiting - Prostate Cancer Clinical Trials

Focal Therapy for Prostate Cancer Using HIFU

INDEX
Start date: June 29, 2011
Phase: N/A
Study type: Interventional

RATIONALE: Prospective trials using hemi-ablation with high intensity focused ultrasound (HIFU) (Sonablate 500) have demonstrated feasibility, safety, and encouraging functional outcomes and early cancer control with 90% of men achieving trifecta status (no erectile dysfunction, leak-free pad-free continence, cancer control). However, these trials have involved small numbers of patients with men selected for good baseline function. A multi-centre prospective trial within a larger cohort of men that better represents the patient population with prostate cancer (external validity) is required.

NCT ID: NCT00555087 Recruiting - Clinical trials for Erectile Dysfunction

Treatment of Erectile Dysfunction in Hypogonadal Men With Testosterone Undecanoate

Nebidolocal
Start date: May 2007
Phase: Phase 4
Study type: Interventional

The main objective of this study is to evaluate the response of erectile dysfunction in hypogonadotrophic males with Testosterone undecanoate i.m. as per IIEF and the question of the GAQ (Global Evaluation Questionnaire) after 42 weeks of treatment. Secondary Study Objectives - To monitor adverse events and changes in hemoglobin and serum chemistry with: PSA, lipid profile, renal-hepatic profile and glycemia, and control by means of a rectal digital examination. - To Determinate physiologic reconstitution in patients under treatment by means of total and free testosterone dosage.

NCT ID: NCT00313898 Recruiting - Clinical trials for Erectile Dysfunction

Effect of Sildenafil on Quality of Sexual Life in Mild to Normally Sexually Functioning Males

Start date: September 2005
Phase: Phase 4
Study type: Interventional

In clinical practice it is quite common to have sexually active male patients with mild/normal erectile function that are not satisfied with their sexual function. The aim of this study is to evaluate the effect of sildenafil on the quality of sexual function in this group of patients. The endpoint of this study is to define another, different group of patients that may respond positively to treatment with sildenafil.