Erectile Dysfunction Clinical Trial
Official title:
Prostate Stimulation for Sexual Dysfunction
The purpose of this study is to use a device to stimulate the prostate with a goal of helping improve symptoms in men with sexual dysfunction.
The purpose of the study is to use a device to stimulate the prostate. The goal of this is to help men with sexual dysfunction. Sexual dysfunction can include conditions like delayed ejaculation (e.g.takes more than 21 minutes to climax) and can hopefully assist them in achieving faster time to ejaculation (e.g. closer to the median of 5.4 minutes in a "normal" individual) along with erectile dysfunction (e.g. the inability to achieve and sustain an erection). ;
Status | Clinical Trial | Phase | |
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Not yet recruiting |
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Phase 2/Phase 3 | |
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Phase 1 | |
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N/A | |
Withdrawn |
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Phase 1 | |
Withdrawn |
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Efficacy, Safety and Dose-response of Udenafil in Patients With Benign Prostatic Hyperplasia and Erectile Dysfunction
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Phase 2 | |
Recruiting |
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Sagene 2014 - Parkinson's Disease and Erectile Dysfunction
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Phase 4 | |
Completed |
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Phase 3 | |
Completed |
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A Study of Tadalafil in Men With Benign Prostatic Hyperplasia (BPH) and Erectile Dysfunction (ED)
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Phase 3 | |
Completed |
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Bone Marrow Mesenchymal Stem Cells in Erectile Dysfunction (ED)
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Phase 1 | |
Completed |
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Research Evaluating a PDE5 Inhibitor for Erectile Dysfunction
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Phase 4 | |
Not yet recruiting |
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A Study to Evaluate a Possible Superiority Expressed by the Faster Onset of Action and the Efficacy and Safety of Sildenafil Citrate 20mg Sublingual Tablet in the Treatment of Erectile Dysfunction of Different Etiologies
|
Phase 3 | |
Completed |
NCT01230541 -
Effect of Udenafil on Spermatogenesis
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Phase 1 | |
Terminated |
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Pudendal Assessment in Erectile Dysfunction
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N/A | |
Completed |
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Effectiveness of Physiotherapy to Treat the Urinary Incontinence and Erectile Dysfunction Post Retropubic Prostatectomy
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N/A | |
Completed |
NCT01037218 -
Treatment of Erectile Dysfunction II
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Phase 3 | |
Completed |
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Treatment of Erectile Dysfunction I
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Phase 3 | |
Recruiting |
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Phase 4 | |
Completed |
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Evaluating the Efficacy of Vardenafil in Subjects With Erectile Dysfunction (ED) Administered 12, 18 or 24 Hours Prior to Intercourse
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Phase 4 | |
Completed |
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Assessment of Duration of Erection With Vardenafil 10 mg
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Phase 4 | |
Completed |
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Efficacy and Safety of Tadalafil in Subjects With Erectile Dysfunction Caused by Spinal Cord Injury
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Phase 3 |