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PROPPER Prospective Registry of Outcomes With Penile Prosthesis

NCT01383018 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1457

Last updated 2021-02-12

Study results available
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Summary

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.

Conditions

Interventions

DEVICE

AMS Penile Prosthesis Devices

Non-interventional device registry. Outcomes for patients receiving marketed AMS penile prosthesis devices.

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Gerard Henry, MD · Ark-LA-Tek

  • Anthony J. Bella, MD · University of Ottawa

  • Edward Karpman, MD · El Camino Urology Medical Group

  • LeRoy Jones, MD · Urology San Antonio Research PA

  • Bryan T Kansas, MD · The Urology Team

  • Brian Christine, MD · Urology Centers of Alabama

  • Kevin McVary, MD · SIU School of Medicine

  • James Hotaling, MD · University of Utah

  • Mohit Khera, MD · Baylor College of Medicine

  • Eugene Rhee, MD · Kaiser Permanente

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-13
Primary Completion
2017-11-30
Completion
2018-07-25
FDA Device
Yes

Countries

  • United States
  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01383018 on ClinicalTrials.gov