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Study identifier: NCT07053826 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Penile Lengthening Pre-Penile Prosthesis Implantation

Condition: Erectile Dysfunction  ·  Sponsor: University of Pittsburgh

PhaseNA
Planned participants48
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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 prostate surgery. Use of the device has not been shown to have any detrimental effects on sexual or overall health.

This description comes directly from the study's public registry record.

Talk to the study team

Roger D Klein, MD, PhD  ·  800-533-8762  ·  urologyresearch@upmc.edu

Michelle Lucas, MS  ·  412-624-4708  ·  mcmeansmm2@upmc.edu

Always discuss trial participation with your own doctor first.

Locations (1)

UPMC Mercy Hospital, UrologyPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07053826