At a glance
ClinicalIndex Comparison RecordN/ACompleted· 44 enrolled
Drug / intervention
The Prefyx PPS™ Pre-pubic Sling Systemdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
The Prefyx PPS™ System eRegistry
In Brief
An observational study evaluating The Prefyx PPS™ Pre-pubic Sling System for Stress Urinary Incontinence. Completed, enrolled 44 participants across 5 sites.
Detailed Summary
Registry to gather information about the long term use of the Prefyx PPS System for the treatment of Stress Urinary Incontinence (SUI).
Study Details
Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsStress Urinary Incontinence
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartDec 2006
First PostedJun 2008
Primary CompletionNov 2008
Study CompletionApr 2009
TodayJul 2026
First PostedJun 2, 2008
Enrollment StartDec 1, 2006
Primary CompletionNov 1, 2008
Study CompletionApr 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 18.1 years ago
Interventions
The Prefyx PPS™ Pre-pubic Sling Systemdevice
device designed to treat female stress urinary incontinence (SUI).