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Erectile Dysfunction clinical trials

View clinical trials related to Erectile Dysfunction.

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NCT ID: NCT00817830 Withdrawn - Clinical trials for Erectile Dysfunction

Cardiovascular Safety Study of Lodenafil Carbonate in Patients With Coronaropathy During Physical Effort

Start date: November 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to assess the safety of lodenafil carbonate in patients with coronaropathy, evaluating the response of the body facing physical effort, including both heart and respiratory components, with and without use of lodenafil carbonate 80mg.

NCT ID: NCT00814736 Completed - Clinical trials for Erectile Dysfunction

A Randomized, Double-Blinded, Placebo-Controlled, Two-Way Crossover Study to Investigate the Safety and Toleration of Single Dose Sildenafil in Subjects Receiving Chronic UK-369,0031

Start date: August 2008
Phase: Phase 1
Study type: Interventional

To investigate the safety and overall tolerability of co-administration two PDE5 inhibitors UK369,003 and sildenafil

NCT ID: NCT00809471 Completed - Clinical trials for Erectile Dysfunction

Research Evaluating an Investigational Medication for Erectile Dysfunction - Diabetic ED (REVIVE-D)

REVIVE-D
Start date: December 2008
Phase: Phase 3
Study type: Interventional

This study is being conducted to compare the safety and efficacy of 2 doses of avanafil to placebo in diabetic men with mild to severe erectile dysfunction.

NCT ID: NCT00795938 Completed - Clinical trials for Erectile Dysfunction

Study to Compare the Blood Levels of Sildenafil Following Administration of an Experimental Tablet vs. the Conventional Oral Tablet in Healthy Subjects.

Start date: October 2008
Phase: Phase 1
Study type: Interventional

This study to will compare the blood levels of sildenafil following administration of an experimental tablet vs. the conventional oral tablet.

NCT ID: NCT00790751 Completed - Clinical trials for Erectile Dysfunction

Research Evaluating an Investigational Medication for Erectile Dysfunction - General ED

REVIVE
Start date: November 2008
Phase: Phase 3
Study type: Interventional

This study is being conducted to compare the safety and efficacy of 3 doses of avanafil to placebo in men with mild to severe erectile dysfunction.

NCT ID: NCT00786253 Completed - Clinical trials for Erectile Dysfunction

Sustainable Efficacy of Vardenafil OD Versus Vardenafil PRN in Erectile Dysfunction

Start date: October 2005
Phase: Phase 2
Study type: Interventional

Compare once daily vs on demand treatment in men with erectile dysfunction. Treatment of mild to moderate erectile dysfunction with 10 mg vardenafil p.o. over 24 weeks + 4 weeks wash-out: A: once daily at bedtime for 12 weeks followed by 12 weeks of placebo B: once daily at bedtime for 24 weeksC: PRN for 24 weeks

NCT ID: NCT00777075 Completed - Clinical trials for Erectile Dysfunction

L-Arginine and Erectile Dysfunction

Start date: July 2003
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine whether the treatment with L-arginine leads to an improvement of erectile dysfunction in patients with erectile dysfunction.

NCT ID: NCT00770042 Completed - Clinical trials for Erectile Dysfunction

To Evaluate The Effect Of Ketoconazole, Ritonavir and Erythromycin on the Safety and Pharmacokinetics of Avanafil

Start date: October 2008
Phase: Phase 1
Study type: Interventional

This study is being conducted to examine the effect of three CYP3A4 inhibitors (ketoconazole, erythromycin and ritonavir) on the single dose pharmacokinetics of avanafil. Ketoconazole and ritonavir are potent inhibitors of CYP3A4 and erythromycin is a moderate CYP3A4 inhibitor. Any interaction that is observed would be predictive of other inhibitors of CYP3A4.

NCT ID: NCT00769041 Completed - Clinical trials for Erectile Dysfunction

A Thorough EKG Safety Study of TA-1790 (Avanafil)

Start date: October 2008
Phase: Phase 1
Study type: Interventional

This study is to assess whether treatment with a therapeutic (100 mg) or supratherapeutic (800 mg) dose of avanafil has the potential to cause QT/QTc prolongation in healthy volunteers.

NCT ID: NCT00743613 Completed - Clinical trials for Peripheral Arterial Disease

Predicting Peripheral Arterial Disease in Men With Erectile Dysfunction

PREPARED
Start date: February 2005
Phase: N/A
Study type: Observational

Erectile dysfunction is a common complaint and is found frequently in men with hyperlipidemia, hypertension, diabetes and those who smoke. ED may also be an early warning of peripheral arterial disease. This study is designed to look for a relationship between the degree of ED and the presence of PAD when associated with co-morbid conditions.