The Prefyx PPS™ System eRegistry

NCT00688181 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2021-03-01

Study results available
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Summary

Registry to gather information about the long term use of the Prefyx PPS System for the treatment of Stress Urinary Incontinence (SUI).

Conditions

  • Stress Urinary Incontinence

Interventions

DEVICE

The Prefyx PPS™ Pre-pubic Sling System

device designed to treat female stress urinary incontinence (SUI).

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Robert Walsh, M.D. · Boston Scientific Corporation

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-12-31
Primary Completion
2008-11-30
Completion
2009-04-30

Countries

  • United States

Study Locations

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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 NCT00688181 on ClinicalTrials.gov