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Terminated Not applicable Interventional

Vesair Clinical Trial

ClinicalTrials.gov ID: NCT04026347

Public ClinicalTrials.gov record NCT04026347. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 2:11 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Evaluation of the Vesair® Bladder Control System for the Treatment of Stress Urinary Incontinence in Post-Menopausal Women

Study identification

NCT ID
NCT04026347
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Solace Therapeutics, Inc.
Industry
Enrollment
158 participants

Conditions and interventions

Interventions

  • Vesair Balloon Device
  • Sham balloon placement Other

Device · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2020
Primary completion
Feb 27, 2022
Completion
Apr 14, 2022
Last update posted
May 12, 2022

2020 – 2022

United States locations

U.S. sites
25
U.S. states
20
U.S. cities
25
Facility City State ZIP Site status
Valley Urogynecology Associates Phoenix Arizona 85016
Scripps Clinic San Diego California 92130
Tri Valley Urology Temecula California 92592
Dr. Sherry Thomas Westlake Village California 91361
Women's Health Specialty Care Farmington Connecticut 06032
Florida Urology Partners Tampa Florida 33615
Meridian Clinical Research / Urological Associates of Savannah Savannah Georgia 31405
WomanCare Arlington Heights Illinois 60004
CMB Research / Basinski and Juran MDs Newburgh Indiana 47630
Regional Urology Shreveport Louisiana 71106
Chesapeake Urology Hanover Maryland 21076
Chesapeake Urology Owings Mills Maryland 21117
Beth Israel Deaconess Medical Center (BIDMC) Boston Massachusetts 02210
Mercy Health Ada Michigan 49301
Freedman Urology Las Vegas Nevada 89144
ProHEALTH Garden City Urology Garden City New York 11530
Premier Medical Group of the Hudson Valley Poughkeepsie New York 12601
Associated Urologists of North Carolina Raleigh North Carolina 27612
MetroHealth Cleveland Ohio 44109
Penn Medicine Philadelphia Pennsylvania 19041
Women and Infants dept of Urogynecology Providence Rhode Island 02903
Houston Metro Urology Houston Texas 77027
Urology San Antonio San Antonio Texas 78229
Urology of Virginia Virginia Beach Virginia 23462
Washington Urology Kirkland Washington 98034

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04026347, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 12, 2022 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04026347 live on ClinicalTrials.gov.

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