We've found
452
archived clinical trials in
Erectile Dysfunction
We've found
452
archived clinical trials in
Erectile Dysfunction
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
A Study of LY900010 in Erectile Dysfunction
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
A Study of LY900010 in Erectile Dysfunction
Updated: 1/1/1970
A Study of LY900010 (LY2452473 + Tadalafil) in the Treatment of Men With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
Avanafil in the Treatment of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter Study of the Safety and Efficacy of Avanafil in the Treatment of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy
Status: Archived
Avanafil in the Treatment of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy
Updated: 1/1/1970
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Multicenter Study of the Safety and Efficacy of Avanafil in the Treatment of Erectile Dysfunction Following Bilateral Nerve-Sparing Radical Prostatectomy
Status: Archived
Updated: 1/1/1970
Pudendal Assessment in Erectile Dysfunction
A Cohort Study of the Functional Significance of Internal Pudendal Artery Stenoses in Patients With Erectile Dysfunction
Status: Archived
Pudendal Assessment in Erectile Dysfunction
Updated: 1/1/1970
A Cohort Study of the Functional Significance of Internal Pudendal Artery Stenoses in Patients With Erectile Dysfunction
Status: Archived
Updated: 1/1/1970
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
PDE5 Inhibitor Use and Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Updated: 12/31/1969
Prospective Case Crossover Study to Assess Whether PDE5 Inhibitor Exposure in Men Increases the Risk for the Development of Non-arteritic Anterior Ischemic Optic Neuropathy (NAION)
Status: Enrolling
Updated: 12/31/1969
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Therapy for Erectile Dysfunction Adaptation of ACT for Compliance With an Erectile Rehabilitation Program
Updated: 12/31/1969
ACT-ED: Acceptance and Commitment Therapy for Erectile Dysfunction Adaptation of ACT for Compliance With an Erectile Rehabilitation Program
Status: Enrolling
Updated: 12/31/1969
Therapy for Erectile Dysfunction Adaptation of ACT for Compliance With an Erectile Rehabilitation Program
Updated: 12/31/1969
ACT-ED: Acceptance and Commitment Therapy for Erectile Dysfunction Adaptation of ACT for Compliance With an Erectile Rehabilitation Program
Status: Enrolling
Updated: 12/31/1969
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Pharmacological Penile Rehabilitation in the Preservation of Erectile Function Following Bilateral Nerve-Sparing Radical Prostatectomy
Updated: 12/31/1969
A Randomized Trial of Pharmacological Penile Rehabilitation in the Preservation of Erectile Function Following Bilateral Nerve-Sparing Radical Prostatectomy
Status: Enrolling
Updated: 12/31/1969
Pharmacological Penile Rehabilitation in the Preservation of Erectile Function Following Bilateral Nerve-Sparing Radical Prostatectomy
Updated: 12/31/1969
A Randomized Trial of Pharmacological Penile Rehabilitation in the Preservation of Erectile Function Following Bilateral Nerve-Sparing Radical Prostatectomy
Status: Enrolling
Updated: 12/31/1969
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L-Arginine Supplementation With or Without Enzyme Inhibitors Treating Erectile Function of Prostate Cancer Survivors
Updated: 12/31/1969
A Randomized Phase II Dose Finding Study of ArginMax for Its Effect on Erectile Function and Quality of Life in Survivors of Prostate Cancer Previously Treated With Radiotherapy
Status: Enrolling
Updated: 12/31/1969
L-Arginine Supplementation With or Without Enzyme Inhibitors Treating Erectile Function of Prostate Cancer Survivors
Updated: 12/31/1969
A Randomized Phase II Dose Finding Study of ArginMax for Its Effect on Erectile Function and Quality of Life in Survivors of Prostate Cancer Previously Treated With Radiotherapy
Status: Enrolling
Updated: 12/31/1969
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Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Status: Enrolling
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Status: Enrolling
Updated: 12/31/1969
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Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Status: Enrolling
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Updated: 12/31/1969
Evaluate the Use of Liposuction and Cell Separation Devices for Autologous Fat (Adipose) Derived Cells to Treat the Symptoms of Erectile Dysfunction
Status: Enrolling
Updated: 12/31/1969
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Safety and Clinical Outcomes Study: SVF Deployment for Orthopedic, Neurologic, Urologic, and Cardio-pulmonary Conditions
Updated: 12/31/1969
Clinical Intervention Study: Adverse Events and Clinical Outcomes for the Deployment of Adipose Derived SVF (Rich in Adult Stem Cells and Growth Factors)for Select Orthopedic, Neurologic, Urologic, and Cardio-Pulmonary Conditions.
Status: Enrolling
Updated: 12/31/1969
Safety and Clinical Outcomes Study: SVF Deployment for Orthopedic, Neurologic, Urologic, and Cardio-pulmonary Conditions
Updated: 12/31/1969
Clinical Intervention Study: Adverse Events and Clinical Outcomes for the Deployment of Adipose Derived SVF (Rich in Adult Stem Cells and Growth Factors)for Select Orthopedic, Neurologic, Urologic, and Cardio-Pulmonary Conditions.
Status: Enrolling
Updated: 12/31/1969
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Improving Erectile Function and Quality of Life After Prostate Cancer Treatment
Updated: 12/31/1969
Improving Erectile Function and Quality of Life After Prostate Cancer Treatment
Status: Enrolling
Updated: 12/31/1969
Improving Erectile Function and Quality of Life After Prostate Cancer Treatment
Updated: 12/31/1969
Improving Erectile Function and Quality of Life After Prostate Cancer Treatment
Status: Enrolling
Updated: 12/31/1969
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DHACM in Robotic Assisted Laparoscopic Prostatectomy (RALP)
Updated: 12/31/1969
A Prospective Randomized Clinical Trial Using Dehydrated Human Amnion/Chorion Membrane (dHACM) in Nerve Sparing Robotic Assisted Laparoscopic Radical Prostatectomy (RALP) - Effect on Potency Outcomes
Status: Enrolling
Updated: 12/31/1969
DHACM in Robotic Assisted Laparoscopic Prostatectomy (RALP)
Updated: 12/31/1969
A Prospective Randomized Clinical Trial Using Dehydrated Human Amnion/Chorion Membrane (dHACM) in Nerve Sparing Robotic Assisted Laparoscopic Radical Prostatectomy (RALP) - Effect on Potency Outcomes
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
PROPPER Prospective Registry of Outcomes With Penile Prosthesis
Updated: 12/31/1969
Prospective Registry of Outcomes With Penile Prosthesis for Erectile Restoration (PROPPER)
Status: Enrolling
Updated: 12/31/1969
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Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
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Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
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Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
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Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Updated: 12/31/1969
A Randomized, Double-Blind, Placebo-Controlled, Open-Label Extension Clinical Trial of the Dornier Aries 2 Extracorporeal Shock Wave Device for the Treatment of Mild Erectile Dysfunction (ED)
Status: Enrolling
Updated: 12/31/1969
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Autologous Bone Marrow Cells in Treatment of Erectile Dysfunction.
Updated: 12/31/1969
Feasibility Study of Intra-cavernosal Administration of Non-Expanded Autologous Bone Marrow Cells in Treatment of Erectile Dysfunction.
Status: Enrolling
Updated: 12/31/1969
Autologous Bone Marrow Cells in Treatment of Erectile Dysfunction.
Updated: 12/31/1969
Feasibility Study of Intra-cavernosal Administration of Non-Expanded Autologous Bone Marrow Cells in Treatment of Erectile Dysfunction.
Status: Enrolling
Updated: 12/31/1969
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ED Recovery in Men Age =65 Treated With Bilateral Nerve Sparing Robotic Assisted Prostatectomy for Prostate Cancer
Updated: 12/31/1969
Erectile Dysfunction Recovery in Men Age =65 Treated With Bilateral Nerve Sparing Robotic Assisted Prostatectomy (BNS-RAP) for Prostate Cancer
Status: Enrolling
Updated: 12/31/1969
ED Recovery in Men Age =65 Treated With Bilateral Nerve Sparing Robotic Assisted Prostatectomy for Prostate Cancer
Updated: 12/31/1969
Erectile Dysfunction Recovery in Men Age =65 Treated With Bilateral Nerve Sparing Robotic Assisted Prostatectomy (BNS-RAP) for Prostate Cancer
Status: Enrolling
Updated: 12/31/1969
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The Incidence and Treatment of Insulin Resistance Among Men With Erectile Dysfunction
Updated: 1/31/2006
The Incidence and Treatment of Insulin Resistance Among Men With Erectile
Status: Enrolling
Updated: 1/31/2006
The Incidence and Treatment of Insulin Resistance Among Men With Erectile Dysfunction
Updated: 1/31/2006
The Incidence and Treatment of Insulin Resistance Among Men With Erectile
Status: Enrolling
Updated: 1/31/2006
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Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Click here to add this to my saved trials
Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Click here to add this to my saved trials
Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Evaluate Improvement of Erectile Dysfunction After Placement of the AMS IPP 2005 Inflatable Penile Prosthesis
Updated: 3/11/2008
A Multi-Center Study to Assess the AMS IPP 2005 Inflatable Penile Prosthesis Cylinders, Pump and Reservoir.
Status: Enrolling
Updated: 3/11/2008
Click here to add this to my saved trials