TENS Analgesia During Outpatient Urethral Bulking for Stress Urinary Incontinence.

Recruiting N/A Interventional Study
Stress Incontinence Female Urinary Incontinence Urinary Incontinence,Stress Pain Pain Acute
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
100 (estimated)
Sponsor
University of Rochester · Other
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About This Trial
This will be a double-blind randomized control trial in women with stress urinary incontinence who are undergoing an outpatient transurethral bulking procedure for stress urinary incontinence. Subjects will be identified by the University of Rochester urologists and urogynecologists participating in the study who currently oversee stress incontinence care. Subjects will be randomized into two grou…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * • Women, Age ≥18 years * Diagnosis of SUI * Scheduled to undergo transurethral bulking in the office * Able to read/write English Exclusion Criteria: * • Cutaneous damage such as ulcers or broken skin on target treatment area * Currently implanted cardiac pacemaker…
Contacts

Jared M Floch, DO, MS

585-895-9301

jared_floch@urmc.rochester.edu

CONTACT

Diego Hernandez-Aranda, MD

585-487-3400

diego_hernandezaranda@urmc.rochester.edu

CONTACT