Vesair Balloon Confirmatory Trial (VECTOR)

Solace Therapeutics

Status

Terminated

Conditions

Stress Urinary Incontinence

Treatments

Device: Vesair Balloon

Study type

Interventional

Funder types

Industry

Identifiers

NCT03794206

CD1009

Details and patient eligibility

About

Multicenter, prospective, single-arm study to assess the safety and efficacy of the Vesair Bladder Control treatment in post-menopausal women with Stress Urinary Incontinence (SUI) with follow-up at 1, 3 and 12 months. All subjects will be prospectively treated after the subject has provided informed consent and determination that all study entry criteria have been met.

Enrollment

20 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

Previously treated with Vesair Balloon within the past 4 years
Normal voiding function
Has signed consent
Willing to undergo cystoscopy
Available for minimum of 12 months

Exclusion criteria

Last Menstrual Period within past 4 years
Systemic birth control medication (including implants) or systemic hormone replacement therapy (estrogen or progesterone) in the past 4 years.
History of urosepsis, bladder infection, urinary tract infection or asymptomatic bacteriuria within the past 3 months.
Urinary incontinence of neurogenic etiology.
Prior pelvic surgery that may affect incontinence symptoms (including placement and/or removal of a suburethral sling) within the past 4 years.
Noninvasive treatment for incontinence, such as nerve stimulation, Botox injections, biofeedback, formal pelvic floor muscle training, and/or vaginal laser therapy, within the past 3 months.
Taken medications other than anticholinergics that may affect SUI symptoms (such as enobosarm, duloxetine or imipramine) in the past 3 months.
Taking other pharmacologic agents that may have a significant effect on bladder function unless on the therapy for at least 3 months and intending to continue the same dosage of the medication throughout the trial.
History of recurrent (>1) kidney stones, or one kidney stone within the past 5 years.
History of an artificial urinary sphincter.
Presence of gross hematuria and/or blood clots in the urine.
History of interstitial or follicular cystitis or other painful bladder syndrome.
Cystocele verified as Stage 3 or higher by PoP-Q Classification.
Local genital skin infection.
Urethral or bladder inflammation and/or edema, or other hypersensitivity to cystoscopy or other urethral manipulations.
Evidence of involuntary detrusor contractions and/or discomfort during bladder filling up to 300cc.
Undergoing or anticipating a course of pelvic radiation therapy or with severe pelvic fibrosis from previous radiation therapy.
Non-ambulatory, bedridden or physically unable to complete test exercises.
History of recent alcoholism or illicit drug abuse within the last year.
Immunologically suppressed or immunocompromised.
History of any neurological disease that could impact bladder function including Parkinson's disease, multiple sclerosis or post-stroke sequelae.
Uncontrolled diabetes (persistent A1C levels >9 percent).
History of any malignancy (except non-melanoma skin cancer), unless the cancer was not in the urinary tract, the cancer was stage II or less, the cancer was treated with curative intent, AND there have been no clinical signs or symptoms of the malignancy for at least 2 years.
Morbid obesity, defined as BMI ≥40.0.
History of any autoimmune or connective tissue disease or disorder that could impact bladder function