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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 Oct 25, 2026, 11:55 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Single-blind, multicenter, randomized clinical trial of the Vesair Balloon in 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

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
Feb 1, 2020 (Actual)
Primary completion
Feb 28, 2022 (Actual)
Completion
Apr 15, 2022 (Actual)
Last update posted
May 13, 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 13, 2022 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04026347 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →