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Completed Not applicable Interventional

Solace Stress Urinary inContinence Control Efficacy and Safety Study

ClinicalTrials.gov ID: NCT02210273

Public ClinicalTrials.gov record NCT02210273. 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 Jun 26, 2026, 8:03 AM EDT

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

Official title

Evaluation of the Solace Bladder Control System in the Treatment of Female Subjects With Stress Urinary Incontinence

Study identification

NCT ID
NCT02210273
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Solace Therapeutics, Inc.
Industry
Enrollment
221 participants

Conditions and interventions

Interventions

  • Solace Bladder Control (Vesair) Balloon Device
  • Solace Sham Treatment Device

Device

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
Aug 10, 2014
Primary completion
Dec 17, 2015
Completion
Mar 29, 2019
Last update posted
Jul 9, 2019

2014 – 2019

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Valley Urogynecology Associates Phoenix Arizona 85016
Urological Associates of Southern Arizona Tucson Arizona 85715
Genitourinary Surgical Consultants Denver Colorado 80220
Urology Associates of Norwalk Norwalk Connecticut 06850
WomanCare Arlington Heights Illinois 60004
Women's Health Institute of Illinois Oak Lawn Illinois 60453
Regional Urology Shreveport Louisiana 71106
Chesapeake Urology Glen Burnie Maryland 21061
Chesapeake Urology Owings Mills Maryland 21117
Female Pelvic Medicine and Urogynecology Institute of Michigan Grand Rapids Michigan 49503
North Shore LIJ Great Neck New York 11021
Premier Medical Group Newburgh New York 12550
Premier Medical Group Poughkeepsie New York 12601
Lyndhurst Clinical Research Winston-Salem North Carolina 27103
Women and Infants Hospital Providence Rhode Island 02905
MUSC Urology Charleston South Carolina 29425
Sanford Female Pelvic Medicine and Reconstructive Surgery Clinic Sioux Falls South Dakota 57105
Virginia Women's Center Richmond Virginia 23233
Urology of Virginia Virginia Beach Virginia 23462
Integrity Medical Research Mountlake Terrace Washington 98043

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 NCT02210273, 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 Jul 9, 2019 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02210273 live on ClinicalTrials.gov.

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