# Post Market Clinical Study to Evaluate a Mid-Urethral Vaginal Tape Procedure With a Pre-Pubic Delivery Approach, for the Treatment of Stress Urinary Incontinence

> **NCT00688298** · NA · COMPLETED · sponsor: **Boston Scientific Corporation** · enrollment: 100 (actual)

## Conditions studied

- Stress Urinary Incontinence
- Intrinsic Sphincter Deficiency

## Interventions

- **DEVICE:** Prefyx PPS™ System
- **DEVICE:** Advantage ™ System

## Key facts

- **NCT ID:** NCT00688298
- **Lead sponsor:** Boston Scientific Corporation
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2004-05
- **Primary completion:** 2007-03
- **Final completion:** 2008-03
- **Target enrollment:** 100 (ACTUAL)
- **Last updated:** 2020-11-12


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00688298

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00688298, "Post Market Clinical Study to Evaluate a Mid-Urethral Vaginal Tape Procedure With a Pre-Pubic Delivery Approach, for the Treatment of Stress Urinary Incontinence". Retrieved via AI Analytics 2026-08-23 from https://api.ai-analytics.org/clinical/NCT00688298. Licensed CC0.

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