The Prefyx PPS™ System eRegistry

Completed

Conditions studied: Stress Urinary Incontinence

In brief

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

Key facts

Study ID

NCT00688181

Run by

Boston Scientific Corporation

People needed

44

Starts

2006-12-01

Expected to finish

2009-04-01

Last updated by the study team

2021-03-01

Who can join

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

You may qualify if…

• Patients presenting for treatment of female Urinary Stress Incontinence (SUI)

You may not qualify if…

• Pregnant patients, patients with the potential for future growth or patients that are considering future pregnancies.
• Any patients with soft tissue pathology into which the implant is to be placed.
• Patients with any pathology which would compromise implant placement.
• Patients with any pathology, such as blood supply limitations or infections that would compromise healing.

Where it is running

• South Florida Urology Center — Pembroke Pines, Florida, United States
• OB/GYN Specialists of the Palm Beaches — West Palm Beach, Florida, United States
• Urology Specialists of Atlanta, LLC /Northside Hospital — Atlanta, Georgia, United States
• Affiliates in Urology — Westland, Michigan, United States
• HillCrest Medical Center — Tulsa, Oklahoma, United States

Full record on ClinicalTrials.gov

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