Penile Lengthening Pre-Penile Prosthesis Implantation

Stopped early · Not applicable

Conditions studied: Erectile Dysfunction

In brief

This study is intended to utilize a novel, class I (ie. lowest risk, clinical studies not required) medical device to determine whether penile length can be increased in men prior to undergoing a penile prosthesis implantation procedure.

Key facts

Study ID

NCT03500406

Run by

Mayo Clinic

People needed

24

Starts

2018-03-23

Expected to finish

2019-04-01

Last updated by the study team

2020-01-06

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Men undergoing placement of a penile prosthesis
• Must be the first time a penile prosthesis is implanted
• Undergoing implantation of a 3-piece inflatable penile prosthesis

You may not qualify if…

• Prior ischemic priapism
• Any prior penile prosthesis surgeries
• Any prior penile surgeries other than circumcision
• Undergoing malleable penile prosthesis or Ambicor device

Where it is running

• Mayo Clinic in Rochester — Rochester, Minnesota, United States
• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.