NCT00688181

The Prefyx PPS™ System eRegistry

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 44 (actual)
• Sponsor: Boston Scientific Corporation · Industry
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

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

Detailed description

Registry to gather information about the long term use of the Prefyx PPS System which utilizes a pre-pubic surgical approach (device is to be placed in front of the pubic bone) for the treatment of SUI. No additional procedures are required beyond the physician's standard of care.

Conditions

• Stress Urinary Incontinence

Interventions

Type	Name	Description
DEVICE	The Prefyx PPS™ Pre-pubic Sling System	device designed to treat female stress urinary incontinence (SUI).

Timeline

• Start date: 2006-12-01
• Primary completion: 2008-11-01
• Completion: 2009-04-01
• First posted: 2008-06-02
• Last updated: 2021-03-01
• Results posted: 2021-03-01

Locations

5 sites across 1 country: United States