Penile Lengthening Pre-Penile Prosthesis Implantation

Recruiting N/A Interventional Study
Erectile Dysfunction
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Male
Study type
Interventional
Purpose
Treatment
Participants needed
48 (estimated)
Sponsor
University of Pittsburgh · Other
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About This Trial
The goal of this study is to determine whether or not the use of a penile traction therapy device known as RestoreX prior to implantation of a penile prosthesis can increase the length of the implant used during surgery. The device used in this study is commercially available and has been used successfully to facilitate penile lengthening in patients with diabetes and after a certain type of prost…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Have a documented diagnosis of erectile dysfunction * Can provide informed consent * Are willing and able to comply with study procedures and visit schedules * Are to be scheduled for a planned standard of care implantation of an inflatable penile prosthesis Exclusion Criteri…
Contacts

Roger D Klein, MD, PhD

800-533-8762

urologyresearch@upmc.edu

CONTACT

Michelle Lucas, MS

412-624-4708

mcmeansmm2@upmc.edu

CONTACT