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Active clinical trials for "Erectile Dysfunction"

Results 191-200 of 562

Pentoxifylline, Atorvastatin, and Vitamin E in Treating Patients With Erectile Dysfunction After...

Male Erectile DisorderProstate Adenocarcinoma3 more

This phase II trial studies how well pentoxifylline, atorvastatin, and vitamin E (PAVE) work in treating patients with erectile dysfunction after radiation therapy for prostate cancer. Atorvastatin may reduce high cholesterol. Pentoxifylline and vitamin E may enhance blood flow. Giving PAVE may work better in treating prostate cancer patients with post-radiation therapy erectile dysfunction.

Completed25 enrollment criteria

Safety and Efficacy of TD0025 (Rocket1h) for Treatment of Erectile Dysfunction

Erectile Dysfunction

The purpose of this study is to identify the optimal dose(s) of TD0025 for treatment of erectile dysfunction (phase II) and to investigate if treatment of erectile dysfunction with the optimal dose of TD0025 taken as needed over one month is non-inferior than Sildenafil Citrate taken as needed over one month (phase III)

Completed11 enrollment criteria

Daily Avanafil for Erectile Dysfunction

Erectile Dysfunction

In this study, the investigators tried to study the effect of daily avanafil on the serum level of endothelial function markers, as well as its impact on the erectile function in males with erectile and endothelial dysfunction by comparing the results with controls who received placebo.

Completed3 enrollment criteria

A Comparative Pharmacokinetic and Pharmacodynamic Study of Sildenafil in Adult Smokers and Non Smokers...

Erectile DysfunctionSmoking2 more

Smokers are at higher risk of developing Erectile dysfunction (ED) independent of age and comorbidities. Sildenafil is a cytochrome p3A4 (CYP3A4) substrate used for enhancing the erectile function in males. The study purpose is to determine the effect of smoking on male sexual function based on the international index of erectile function score (IIEF) and investigate the effect of smoking (Cigarettes or marijuana) on the pharmacokinetics and pharmacodynamics of sildenafil.

Completed24 enrollment criteria

An Open-Label Study of the Long-Term Safety of Dapoxetine HCl in the Treatment of Rapid Ejaculation...

EjaculationErectile Dysfunction1 more

The purpose of this study is to evaluate the long-term safety of dapoxetine in men with rapid ejaculation.

Completed7 enrollment criteria

POMx In the Treatment of Erectile Dysfunction

Erectile Dysfunction

POMx can be used as a treatment for erectile dysfunction.

Completed16 enrollment criteria

A Bioavailability Study of LY2452473 and Tadalafil

Erectile Dysfunction

This study compares LY2452473 taken orally as a 5 milligram (mg) capsule at the same time as a 5 mg tadalafil tablet with three different combination tablets (LY900010) of 5 mg LY2452473 and 5 mg tadalafil taken orally. The study will evaluate the amount of LY2452473 and tadalafil circulating in the blood for each treatment. Side effects will be documented. This study is approximately 34 days not including screening.

Completed31 enrollment criteria

Drug Interaction Study of Avanafil and Enalapril or Amlodipine

Erectile Dysfunction

The purpose of this study is to determine the change in the blood pressure and pulse rate, pharmacokinetics and the safety when avanafil is taken with either enalapril or amlodipine.

Completed31 enrollment criteria

Phase III Study to Assess the Efficacy and Safety of SK3530 in Patients With Erectile Dysfunction...

Erectile Dysfunction

The purpose of this study is to evaluate the efficacy and safety of SK3530 in men with ED and hypertension who were taking antihypertensive medication.

Completed7 enrollment criteria

A Multicenter, Double-blind Study to Evaluate the Effect of Pretreatment With a Daily Dose of Sildenafil...

Erectile DysfunctionDiabetes Mellitus1 more

To determine the effect on erectile function in a population of type 2 diabetic men with erectile dysfunction who have undergone the following treatment regimen: pre-treatment with a daily dose of double-blind sildenafil versus placebo for 4 weeks (Phase I) followed by an as-needed, flexible-dose, open-label treatment phase with sildenafil for 12 weeks (Phase II). To assess safety and tolerability of this dosing regimen and to investigate its effects on endothelial function and subject's responses to the Self-Esteem And Relationship (SEAR) questionnaire.

Completed2 enrollment criteria
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