Electrostimulation in the Treatment of Idiopathic Overactive Bladder

Janaina Mayer de Oliveira Nunes

Status: Terminated

Conditions: Urinary Bladder, Overactive

Treatments: Other: electrostimulation

Study type: Interventional

Funder types: Other

Identifiers

NCT03519126

Overactive bladder

Details and patient eligibility

About

This is a clinical trial whose objective is to compare the efficacy of transcutaneous electrostimulation of the posterior tibial nerve with intravaginal electrostimulation in the treatment of women with symptoms of idiopathic overactive bladder. The volunteers will be randomly randomized into three study groups: posterior tibial group, vaginal group and control group. They are evaluated at three times: before the start of treatment, at the end of 6 weeks of treatment and after 1 month (follow up). The evaluation will occur through a voiding diary and a quality of life questionnaire. For the treatment groups will be used depolarized biphasic current with frequency of 10 Hz and pulse width of 200 μs, and intensity according to the tolerance of the patient. The hypothesis of the study is that the two forms of electrostimulation for treatment of idiopathic overactive bladder will be effective, but transcutaneous electrostimulation of the posterior tibial nerve will be more effective than intravaginal.

Full description

Objective: To compare the efficacy between intravaginal and transcutaneous electrostimulation of the posterior tibial nerve in the treatment of women with symptoms of idiopathic overactive bladder or mixed urinary incontinence.

METHODS: This is a randomized, controlled, single-blind clinical trial with comparative analysis between study groups and a control, performed at three moments: pre and post clinical intervention and one month after the end of treatment. Vaginal electrostimulation group (GV), transcutaneous electrostimulation group of the posterior tibial nerve (GTP) and control group (CG - without intervention). The intervention groups will be treated with biphasic current with a frequency of 10 Hz and a pulse width of 200 μs for 12 sessions of 30 minutes each. Participants will be evaluated and reevaluated by means of a general data questionnaire, 3-day urinary diary and an International Consultation on Incontinence Questionnaire Overactive Bladder (ICIQ-OAB). Statistical analysis will be performed using SPSS version 22 and the level of significance adopted will be p <0.05.

Enrollment: 67 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Women
• aged 18 years and over
• literate
• exhibit symptoms of overactive bladder (urinary urgency, urge incontinence, nocturia and polaciuria) or mixed urinary incontinence with predominance of urge incontinence
• to present lower urinary tract dysfunction identified by scores that were equal or higher than 8 points in the Overactive Blader version 8 questionnaire (OAB-V8)
• accept to participate in the study by means of signing the Term of Free and Informed Consent approved by the Research Ethics Committee of the University Hospital of the Northern Region of Paraná State University of Londrina (HURNP / UEL).

Exclusion criteria

• Women who are virgin
• pregnant
• have a recurrent lower urinary tract infection (more than three episodes a year)
• vaginal infection
• history of overactive bladder medication in the last three months
• urinary incontinence to efforts exclusively
• previous surgery to treat incontinence urinary
• neurological diseases (such as multiple sclerosis, Alzheimer's disease, stroke, Parkinson's disease)
• current history of genitourinary neoplasia
• genital prolapse above third degree of Baden and Walker
• decompensated diabetic
• patients with cardiac pacemaker
• metal implant in the ankle and right foot
• cognitive deficit that inability to respond to questionnaires properly and / or correctly fill in the voiding diary
• do not perform all treatment sessions

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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67 participants in 3 patient groups

vaginal

Experimental group

Description:

Group of volunteers who will be treated with vaginal electrostimulation

Treatment:

Other: electrostimulation

posterior tibial nerve

Experimental group

Description:

Group treated with transcutaneous electrostimulation of the posterior tibial nerve

Treatment:

Other: electrostimulation

control

No Intervention group

Description:

Group of volunteers who will not be treated