Intravaginal Electrical Stimulation in Idiopathic Overactive Bladder
Idiopathic Overactive Bladder, Electrical Stimulation, Bladder Training
About this trial
This is an interventional treatment trial for Idiopathic Overactive Bladder
Eligibility Criteria
Inclusion Criteria:
- Women over the age of 18 with clinical diagnosis of idiopathic OAB
- Urodynamically diagnosed detrusor overactivity
- The strength of pelvic floor muscle 3/5 and more
- Able to give written, informed consent
- Able to understand the procedures, advantages and possible side effects
- Willing and able to complete the voiding diary and QoL questionnaire
Exclusion Criteria:
- History of conservative therapy (BT, ES) for OAB within 3 months
- Previously treated with antimuscarinics (within 4 weeks)
- Pregnancy or intention to become pregnant during the study
- Current vulvovaginitis or urinary tract infections or malignancy
- History of urogynecological surgery within 3 months
- Anatomic structural disorders of genital region that could not allow to apply the vaginal probe
- Having stage 2 or more according to the pelvic organ prolapse quantification
- Cardiac pacemaker or implanted defibrillator
- Neurogenic bladder, signs of neurologic abnormalities at objective examination; history of the peripheral or central neurologic pathology
- Ultrasonographic evidence of residual urine volume more than 100 ml
- Allergy to condom or lubricant gel that is used with perineometer/vaginal probe
Sites / Locations
- Hakan Alkan
Arms of the Study
Arm 1
Arm 2
Other
Active Comparator
Group 1: Bladder Training - Control group
Group 2: Bladder Training+Intra Vaginal Electrical Stimulation
Specific goals are to correct faulty habit patterns of frequent urination, improve control over bladder urgency, prolong voiding intervals, increase bladder capacity, reduce incontinence episodes and restore patient confidence in controlling bladder function
IVES was performed in lithotomy position via Enraf Nonius Myomed 632 device with a vaginal probe. IVES sessions were performed three times in a week, for 8 weeks. Every session lasted 20 minutes. The intervention comprised a 24-session treatment program of ES. The stimulation parameters were frequency at 10 Hz, a 5-10s work-rest cycle and 100 ms pulse width. The symmetric biphasic pulse wave could be delivered over a range of 0-100 mA. The intensity was controlled according to patients' discomfort level feedback