Comparison of the Efficacy of Perineal and Intravaginal Electrical Stimulation in Women With Idiopathic Overactive Bladder

Exclusion Criteria

• •Women with pure stress urinary incontinence
• •History of conservative treatment for OAB within the last 6 months (MI, IVES, perineal ES, etc.)
• •Pregnant or planning to become pregnant at the time of the study
• •Diagnosis of vaginal infection, urinary tract infection, or cancer
• •Women with urinary incontinence within the last 3 months Those who have undergone urogynecological surgery
• •Those with genital area disorders that may preclude the use of a vaginal probe or perineal electrode
• •Those diagnosed with stage 2 or higher according to the Pelvic Organ Prolapse Assessment (POP-Q)
• •Those with a pacemaker or implanted defibrillator
• •Those with neurogenic bladder or a history of neurological disease
• •Those with a urine residual of more than 100 ml detected by ultrasound (using an ultrasound device)
• •Those with allergies to condoms or lubricating gels used with a vaginal probe or perineometer