Clinical Trials Directory

Trials / Terminated

TerminatedNCT01811797

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

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
Phase
N/A
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Initia · Industry
Sex
Male
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICELow Intensity Shockwave by Renova
DEVICESham treatmentSham treatment that looks, sounds and feels like the real LISW treatment.

Timeline

Start date
2013-10-01
Primary completion
2014-06-01
Completion
2014-06-01
First posted
2013-03-15
Last updated
2015-05-12

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01811797. Inclusion in this directory is not an endorsement.