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Erectile Dysfunction clinical trials

View clinical trials related to Erectile Dysfunction.

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NCT ID: NCT03600766 Active, not recruiting - Clinical trials for Erectile Dysfunction

Mirabegron for Treatment of Erectile Dysfunction in Patients With LUTS Secondry to BPH: A Randomized Study

Start date: August 1, 2018
Phase: Phase 2
Study type: Interventional

To study the impact of mirabegron, a B3-adrenoceptor agonist, in the treatment of ED in patients with LUTS secondary to BPH and concomitant ED.

NCT ID: NCT02446808 Active, not recruiting - Clinical trials for Urinary Incontinence

Intraoperative Nerve Monitoring During Robot-assisted Laparoscopic Prostatectomy

Start date: June 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the use of intraoperative nerve monitoring during robotic-assisted laparoscopic prostatectomy surgery improves post-surgery urinary continence and erectile function.

NCT ID: NCT02443090 Active, not recruiting - Clinical trials for Erectile Dysfunction

Safety and Efficacy Study of Oral Fispemifene for the Treatment of Sexual Dysfunction in Hypogonadal Men

Start date: May 2015
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of fispemifene in men with secondary hypogonadism and sexual side effects.

NCT ID: NCT01601353 Active, not recruiting - Clinical trials for Erectile Dysfunction

Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction

Start date: May 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of adipose derived cells for the treatment of erectile dysfunction symptoms.

NCT ID: NCT00906269 Active, not recruiting - Prostatic Neoplasms Clinical Trials

Can Hyperbaric Oxygen Improve Erectile Function Following Surgery for Prostate Cancer

HBOT
Start date: July 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if adding hyperbaric oxygen therapy, a therapy that delivers oxygen under slight pressure, to a drug treatment of PDE5I (such as Viagra, Levitra, Cialis)for men following surgery for prostate cancer will result in more men being able to continue to have erections.

NCT ID: NCT00582231 Active, not recruiting - Clinical trials for Erectile Dysfunction

Penile Injection Anxiety

Start date: February 2007
Phase:
Study type: Observational

The purpose of this study is to help us understand more about your experience with penile injection therapy. Many men become anxious when thinking about penile injections. We would like to understand more about this anxiety. You will be asked to fill out questionnaires before you start penile injection training, at each training visit, and then at your four month follow-up visit.

NCT ID: NCT00573209 Active, not recruiting - Clinical trials for Erectile Dysfunction

Energy Specific Far Infrared Radiation Treatment for Erectile Dysfunction

Start date: August 2007
Phase: Phase 1
Study type: Interventional

A preliminary study to determine the possibility of using far infrared (FIR) radiation to treat impotency.

NCT ID: NCT00507286 Active, not recruiting - Clinical trials for Erectile Dysfunction

Efficacy and Safety Study of Combined Oral and Injection Therapy for Erectile Dysfunction

Start date: May 2007
Phase: N/A
Study type: Interventional

Erectile dysfunction (ED or impotence) is a common medical condition affecting many men world wide. The most commonly used treatment for ED are oral medications like Viagra (sildenafil), Levitra (vardenafil) and Cialis (tadalafil). If these are not effective the use of an injection into the penis (intracavernosal injection or ICI) is necessary. However in some men neither of these therapies is successful. Hypothesis: An adequate erection may be achieved in men with difficult-to-treat erectile dysfunction, when they are treated with a therapy of combination of tablet and penile injection, when a single treatment therapy has failed for these men. Aim of the study is to test the safety and efficacy of a combination of Viagra and Caverjet Impulse in a group of men who had failed to achieve an adequate response to the maximum recommended dose of either Viagra, Cialis or Levitra and Caverjet Impulse, when these treatments were used alone. 20 men with difficult to treat ED will be given oral medication, intracavernosal therapy or the combination in a single-blind randomised study. Informed consent will be signed prior to any study procedures being carried out. All participants are 'blinded' to their study treatments. Participants who have satisfactory response to any of the tablets or penile injections, will be excluded from the study.

NCT ID: NCT00463957 Active, not recruiting - Clinical trials for Erectile Dysfunction

The Pharmacological Basis for the Increase in Visual Time Constants Induced by Single Oral Doses of Sildenafil

Start date: August 2006
Phase: N/A
Study type: Interventional

Sildenafil and similar drugs have been used for several years to treat erectile dysfunction. It has been noticed that in some people, sildenafil causes a subtle increase in the length of time that visual images that we see are retained by the retina. It is thought that this might be due to an effect of sildenafil on inhibiting an enzyme called phosphodiesterase type 6 (PDE6) which is present in the retina. By giving single oral doses of sildenafil and a similar drug called tadalafil which has less effect on PDE6, we hypothesise that this is the mechanism of the change in vision caused by sildenafil. By performing computerised visual test, we plan to compare the effects of sildenafil, tadalafil and placebo tablets on vision in healthy volunteers.