Vesair Continued Access Trial
Status: | Completed |
---|---|
Conditions: | Urology, Urology |
Therapuetic Areas: | Nephrology / Urology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/17/2019 |
Start Date: | March 9, 2017 |
End Date: | January 15, 2019 |
Vesair Continued Access Trial: Use of the Vesair® Bladder Control System in the Treatment of Post-Menopausal Female Subjects With Stress Urinary Incontinence
Single arm study of the Vesair Balloon in postmenopausal women.
All women enrolled will be treated with the vesair balloon and followed for a maximum of 3
years, with balloon replacement annually.
years, with balloon replacement annually.
Inclusion Criteria:
- Post-menopausal women with SUI or stress predominant mixed incontinence
- Maximum score on IQOL of 60
- Positive cough test for leakage
- Willing to undergo procedures
- Free from infection
- Have previously tried (and failed) noninvasive treatment for SUI
Exclusion Criteria:
- SUI due to SUI
- Urge-predominant mixed incontinence
- Incontinence of neurogenic etiology
- 2 or more UTIs in past year and 1 in past 3 months
- Surgery for SUI in the past 6 months
- taking medication that can be used to treat SUI
- taking medication that affects urinary symptoms for less than 3 months
- undergoing biofeedback
- Grade 3 or worse cystocele
- last menstrual period within 12 months
- oral progesterone or estrogen in the past 12 months
- BMI > 40
- involuntary detrusor contractions or discomfort during bladder filling
- previous stage III or worse cancer
- previous cancer of the urinary tract
- previous symptoms for early stage cancer in the past 2 years
- anticoagulation therapy other than aspirin
- history of prosthetic heart valve
- neurological or connective tissue condition or disease affecting bladder function
- known allergy to device components
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