Solace Stress Urinary inContinence Control Efficacy and Safety Study



Status:Active, not recruiting
Conditions:Urology, Urology
Therapuetic Areas:Nephrology / Urology
Healthy:No
Age Range:18 - Any
Updated:4/5/2019
Start Date:August 11, 2014
End Date:March 30, 2019

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

The SUCCESS Trial is designed to determine whether the Solace Bladder Control System is safe
and effective for the treatment of Stress Urinary Incontinence (SUI) in adult females.

Subject will undergo treatment with the Solace Bladder Control System or a sham procedure,
with the results being compared at 3 months.

All patients undergoing sham treatment are treated at 3 months.

Inclusion Criteria:

- Female 18 years of age or older with stress urinary incontinence (SUI)

- Experienced SUI for at least 12 months and attempted and failed prior noninvasive
treatment

- Willing to undergo cystoscopic procedures required and 36 month follow-up

- On stable medication for a minimum of 3 months

- Free of local genital skin infection

- Positive Pad Weight Test

- Free of impassable urethral strictures, trauma or necrosis

Exclusion Criteria:

- Pregnant or planning to become pregnant during the study period

- Non-ambulatory or bedridden or physically unable to complete test exercises

- Morbidly obese (defined as BMI ≥ 40 kg/m2)

- Incontinence of neurogenic etiology

- Urge predominant Mixed Incontinence

- Bladder infection (including bladder inflammation or edema) or Urinary Tract Infection
(UTI) within 3 months

- History of recurrent urinary tract infections

- Prior surgical procedure for incontinence within the past 6 months

- Is taking medications for urinary incontinence other than anticholinergics

- History of recurrent (>1) or recent (within 5 years) kidney stone(s)

- Has a prosthetic heart valve

- Unable to tolerate any form of antibiotic

- Taking anticoagulation therapy, other than aspirin

- Has urinary incontinence due to Intrinsic Sphincter Deficiency (ISD)
We found this trial at
20
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Denver, Colorado 80220
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Arlington Heights, Illinois 60004
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Arlington Heights, IL
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Charleston, South Carolina 29425
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Charleston, SC
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Glen Burnie, Maryland 21061
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Glen Burnie, MD
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Grand Rapids, MI
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Great Neck, New York 11021
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Great Neck, NY
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Mountlake Terrace, Washington 98043
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Newburgh, New York 12550
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Newburgh, NY
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Norwalk, Connecticut 06859
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Norwalk, CT
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Oak Lawn, Illinois 60453
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Oak Lawn, IL
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Owings Mills, Maryland 21117
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Owings Mills, MD
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Phoenix, Arizona 85016
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Poughkeepsie, New York 12601
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Poughkeepsie, NY
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Providence, Rhode Island 02905
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Providence, RI
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Richmond, Virginia 23233
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Richmond, VA
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Shreveport, Louisiana 71106
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Shreveport, LA
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Sioux Falls, SD
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Tucson, AZ
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Virginia Beach, Virginia 23462
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Virginia Beach, VA
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Winston-Salem, North Carolina 27103
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Winston-Salem, NC
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