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Evaluation of the 2005 AMS (American Medical System) IPP (Inflatable Penile Prosthesis)

NCT00636506 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2019-07-22

Study results available
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Summary

The purpose of this study is to evaluate modifications to the AMS 700 Series pump, cylinders, reservoir and rear tip extender design, their impact on ease of use for the patient, and ease of implantation for the physician.

Conditions

Interventions

DEVICE

AMS 700 IPP with MS Pump

AMS 700 Series Inflatable Penile Prosthesis with MS Pump

Sponsors & Collaborators

  • American Medical Systems

    lead INDUSTRY

Principal Investigators

  • L. Dean Knoll, MD · Medical Research Associates of Nasville

  • Gerard D Henry, MD · Regional Urology LLC

  • Daniel Culkin, MD · University of Oklahoma Health Science Center

  • Dana A Ohl, MD · University of Michigan

  • Juan Otheguy, MD · Advanced Research Institute

  • Ridwan Shabsigh, MD · New York Center for Human Sexuality

  • Steven K Wilson, MD · Institute for Urologic Excellence

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-08-31
Primary Completion
2006-02-28
Completion
2008-01-31

Countries

  • United States

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 NCT00636506 on ClinicalTrials.gov