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Vesair Balloon Confirmatory Trial (VECTOR) — VECTOR  

Stress Urinary Incontinence Clinical Trial

Official title:
CD 1009 Rev A Page 1 of 44 23OCT2018 Vesair Balloon Confirmatory Trial (VECTOR) Use of the Next Generation Vesair® Bladder Control System for the Treatment of Stress Urinary Incontinence in Post-Menopausal Women

Clinical Trial Summary

Multicenter, prospective, single-arm study to assess the safety and efficacy of the Vesair Bladder Control treatment in post-menopausal women with Stress Urinary Incontinence (SUI) with follow-up at 1, 3 and 12 months. All subjects will be prospectively treated after the subject has provided informed consent and determination that all study entry criteria have been met.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03794206
Study type Interventional
Source Solace Therapeutics, Inc.
Contact
Status Terminated
Phase N/A
Start date February 11, 2019
Completion date April 28, 2022
View Details
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