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Erectile Dysfunction clinical trials

View clinical trials related to Erectile Dysfunction.

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NCT ID: NCT02063061 Completed - Clinical trials for Erectile Dysfunction

Low-energy Linear Extracorporal Shock Wave Therapy for Erectile Dysfunction.

ESWTvsED
Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether extracorporeal shock wave therapy (ESWT) is an effective treatment for erectile dysfunction.

NCT ID: NCT02059798 Not yet recruiting - Clinical trials for Erectile Dysfunction

Urinary and Sexual Function Before and After Surgical Decompression of Cervical Myelopathy

Start date: March 2014
Phase: N/A
Study type: Observational [Patient Registry]

Hypotheses: Decompressive surgery of cervical myelopathy will improve bladder function. Decompressive surgery of cervical myelopathy will improve sexual function.

NCT ID: NCT02028013 Recruiting - Clinical trials for Erectile Dysfunction

Management of Sexual Dysfunction With Bioresonance Technique

Start date: January 2013
Phase: N/A
Study type: Observational

Bioresonance is the big promise of the medical technology of the future because it stimulates the self-regenerating system of the body by affecting the body`s most essential procedures. The big advantage is that its multiple and there are no harmful side effects. This therapy teaches something to the body what in a younger and healthier state it had already Bioresonance is based on the scientific principle that metabolism within cells is influenced by one's electromagnetic field. We start to use bioresonance technology in management of erectile dysfunction , premature ejaculation, decreased libido.

NCT ID: NCT02005731 Completed - Clinical trials for Vasculogenic Erectile Dysfunction

Low Intensity Extracorporeal Shockwave Therapy for Patients With Erectile Dysfunction

LISW
Start date: November 2012
Phase: N/A
Study type: Observational

This is a prospective, pilot study for assessing the safety and efficacy of the treatments performed with Renova (LI-ESWT) on symptomatic ED patients.

NCT ID: NCT01996852 Terminated - Prostate Cancer Clinical Trials

Improving Erectile Function and Quality of Life After Prostate Cancer Treatment

Start date: July 2013
Phase: N/A
Study type: Interventional

This is a research study of erectile dysfunction (ED) in men diagnosed with prostate cancer. 144 patients and partners will participate in the study. The purpose of this study is to test a new treatment that combines a cognitive-behavioral intervention with medication and a vacuum constrictive device to treat ED. This new treatment consists of multiple therapeutic elements that enhance compliance with medical treatment and increase sexual activity through enhancement of the sensual pleasure of sex and partner support.

NCT ID: NCT01979848 Completed - Prostate Cancer Clinical Trials

MRI Temperature Mapping of the Prostate and Urogenital Pelvis Cooled by an Endorectal Balloon

Start date: June 2013
Phase: N/A
Study type: Observational

Urinary incontinence and sexual dysfunction are potential side effects for men undergoing the successful removal of the cancerous prostate via surgery. Hypothermic cooling via the investigational Endorectal Cooling Balloon has been shown by our group to significantly reduce long term urinary incontinence and may reduce sexual dysfunction in men after robotic prostatectomy, and improve the patient's long term quality of life (QOL). However before successful translation of the endorectal balloon can proceed into the world wide usage, we must understand: 1. How effectively the tissues for continence and sexual function are cooled within the pelvis. 2. What is the capacity of vascularized structures (i.e. the neurovascular bundle) to 'cool sink' or diminish the effective cooling and 3. Determine if the endorectal balloon can be re‐designed for improved QOL outcomes in men. This research study marries two new techniques of Thermal MRI imaging and Endorectal cooling for prostate cancer surgery. MRI is non‐invasive. A simple confirmation of effective hypothermic cooling can be achieved by novel MRI thermal mapping of the cooling gradient as it comprehensively sweeps through the rectum across the urogenital pelvis. MRI with temperature adaptive software can accurately map these gradients with non‐invasive technique, and answer formidable questions of the effectiveness of hypothermic cooling of the prostate and its direct translation into improved continence and sexual function after surgery. The purpose of this research study is to use Magnetic Resonance Imaging (MRI) and Thermal MRI with subjects who will receive the investigational endorectal cooling balloon to help further understand how the cooling balloon works, which may translate to other uses in the future, including the diagnosis of patients at a high risk of developing prostate cancer.

NCT ID: NCT01967264 Completed - Clinical trials for Erectile Dysfunction

Safety and Pharmacokinetic Profile of Udenafil in Healthy Mexican Adults

Start date: July 2013
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of Udenafil 150 mg compared to placebo.

NCT ID: NCT01967251 Withdrawn - Clinical trials for Erectile Dysfunction

Efficacy, Safety and Dose-response of Udenafil in Patients With Benign Prostatic Hyperplasia and Erectile Dysfunction

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

The purpose of this study is to evaluate the efficacy, dose-response and safety of udenafil 25 mg, 50 mg and 75 mg every day (q.d.) for 12 weeks in the treatment of lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH and for the treatment of erectile dysfunction (ED).

NCT ID: NCT01953523 Completed - Osteoarthritis Clinical Trials

Safety and Clinical Outcomes Study: SVF Deployment for Orthopedic, Neurologic, Urologic, and Cardio-pulmonary Conditions

Start date: September 2, 2013
Phase: N/A
Study type: Interventional

To evaluate for any adverse effects that may be related to the administration and reception of autologous adipose derived stromal vascular fraction (SVF). Secondarily, the study monitors the results of subjective and objective findings as it applies to the non-blinded deployment of autologous SVF for various inflammatory and/or degenerative conditions including select orthopedic, neurologic, urologic and cardio-pulmonary conditions. SVF deployments include intra-venous, intra-articular, and soft tissue injections.

NCT ID: NCT01941732 Completed - Clinical trials for Erectile Dysfunction

Motor Response to Sildenafil in PD

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

Sildenafil (Viagra(R))is widely used by men with Parkinsons Disease (PD) and erectile dysfunction. A number of patients have reported that when they take Sildenafil, their need of anti-PD medication is reduced. We hypotheses that sildenafil increases brain blood flow and hence improves the function of specific brain regions, improving motor function. Motor function and cerebral blood flow of 8 patients will be tested before and after Sildenafil intake and before and after anti-PD medication.