PROPPER Prospective Registry of Outcomes With Penile Prosthesis

Completed

Conditions studied: Erectile Dysfunction, Impotence

In brief

The purpose of this observational registry is to collect and better understand "real-world" outcomes for men undergoing penile implant surgery to treat erectile dysfunction.

Key facts

Study ID

NCT01383018

Run by

Boston Scientific Corporation

People needed

1457

Starts

2011-06-13

Expected to finish

2018-07-25

Last updated by the study team

2021-02-12

Who can join

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

You may qualify if…

• Men diagnosed with erectile dysfunction (ED) for whom an AMS penile prosthesis is recommended by their physician are eligible for inclusion. Potentially eligible men should also meet the following inclusion criteria for study enrollment:
• Willing and able to provide written informed consent prior to enrollment (if applicable).
• Willing to be seen or contacted by phone by the investigator and answer at least 2 questions related to satisfaction and device use 1 year following implantation of an AMS penile prosthesis.

You may not qualify if…

• Men who are deemed by their physician to be not suitable for a penile implant will be excluded.

Where it is running

• Urology Centers of Alabama — Homewood, Alabama, United States
• El Camino Urology Medical Group — Mountain View, California, United States
• Kaiser Permanente — San Diego, California, United States
• SIU School of Medicine — Springfield, Illinois, United States
• Ark-LA-Tek — Bossier City, Louisiana, United States
• Lahey Clinic — Burlington, Massachusetts, United States
• The Urology Team — Austin, Texas, United States
• Baylor College of Medicine — Houston, Texas, United States
• Urology San Antonio Research, PA — San Antonio, Texas, United States
• University of Utah — Salt Lake City, Utah, United States
• University of Ottawa — Ottawa, Ontario, Canada

Full record on ClinicalTrials.gov

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