Safety and Efficacy Associated With Treating Erectile Dysfunction Patients With Low Intensity Shockwaves by Renova

Vasculogenic Erectile Dysfunction Clinical Trial

Official title:
A Prospective, Randomized, Double Blind With Sham Control, Clinical Study to Assess the Safety and Efficacy Associated With Treating Patients Suffering From Erectile Dysfunction With Low Intensity Shockwaves by Renova

Status Terminated

Clinical Trial Summary

This is a prospective, randomized, double-blind clinical study comparing safety and efficacy of the treatments performed with the Low Intensity Extracorporeal Shockwave Therapy (LI-ESWT) device - "Renova" on symptomatic ED patients to the safety and efficacy of the control sham patients.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Erectile Dysfunction
Vasculogenic Erectile Dysfunction

Clinical Trial Details

NCT number	NCT01811797
Study type	Interventional
Source	Initia
Contact
Status	Terminated
Phase	N/A
Start date	October 2013
Completion date	June 2014

View Details

See also
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Completed	`NCT02584686` - Intracavernosal Injection of Botulinum Toxin Type A in the Treatment of Vascular Erectile Dysfunction	Phase 1
Completed	`NCT02005731` - Low Intensity Extracorporeal Shockwave Therapy for Patients With Erectile Dysfunction	N/A
Terminated	`NCT02152683` - Linear Focused Shockwave Treatment for Erectile Dysfunction	N/A
Withdrawn	`NCT03843086` - Low Intensity Linear Shockwave Therapy for Erectile Dysfunction	N/A
Completed	`NCT03067987` - Safety and Efficacy of Low Intensity Shockwave for the Treatment of Erectile Dysfunction	N/A
Completed	`NCT01814852` - Low Intensity Extracorporeal Shockwave Therapy (LI-ESWT) by 'Renova' for Patients With Erectile Dysfunction	N/A