Penile Lengthening Pre-Penile Prosthesis Implantation

Overview

About this study

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.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria

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

Exclusion Criteria

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

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status
Rochester, Minn. Mayo Clinic principal investigator Landon Trost, M.D.	Closed for enrollment

Mayo Clinic Location

Status

Rochester, Minn.

Mayo Clinic principal investigator

Landon Trost, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available

Clinical Trials