Assessment of Penile Vibratory Stimulation Using the Viberect in Men With Mild-Moderate ED

Stopped early · Not applicable

Conditions studied: Organic Erectile Dysfunction

In brief

The primary objective of this study is to assess the safety, acceptability, and satisfaction of penile vibratory stimulation in treatment of erectile dysfunction (ED). The secondary objective is to demonstrate subjective physiological response (erection, rigidity, orgasm) after four weeks of frequent device use and the satisfaction of penile erection and sexual intercourse with partner.

Key facts

Study ID

NCT01715571

Run by

Johns Hopkins University

People needed

11

Starts

2013-03-01

Expected to finish

2020-07-01

Last updated by the study team

2021-06-23

Who can join

Age: 30 and older, up to 70. Sex: male. Healthy volunteers: accepted.

You may qualify if…

• mild-moderate erectile dysfunction based on International Index of Erectile Function (IIEF) erectile function score 13-25

You may not qualify if…

• Men with neurological disease
• IIEF score less than 13
• Spinal cord injury
• History of priapism
• Pelvic neuropathy
• Post-prostatectomy
• Penile skin lesions or ulcers
• Inability to understand and demonstrate device use instructions

Where it is running

• Johns Hopkins Hospital — Baltimore, Maryland, United States
• Frederick Urology Specialists — Frederick, Maryland, United States

Full record on ClinicalTrials.gov

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