Voiding dysfunction. Bladder-neck obstruction
Conditions
Interventions
Intervention 1: Intervention group: Real interferential electrical stimulation with a carrier frequency of 4000 Hz and a beat frequency of 80-160 Hz using Novin device (2 channels/made in Iran, Isfaha
however in this group the intensity of the output of the device will be adjusted to the initial sensation of the patient and then after 1 minute, the output of the device will be turn off.
Sponsors
Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Women between 18 and 65 years old Positive urodynamic criteria favor the voiding dysfunction diagnosis. Women who have voiding dysfunction according to urologist diagnosis. Women whose 3-day urinary history has an average visit to the bathroom more than 8 times in 24 hours. Absence of pregnancy and breastfeeding No history of spinal and pelvic surgery in the last 2 years No history of back and pelvic malignancies in the last 2 years Absence of structural disorder, neurological disorder, history of chronic disease Absence of neurologic bladder Absence of voiding dysfunction secondary to drug use or other diseases Absence of high degrees of pelvic organ prolapse (degrees higher than 2) Personal written consent to enter the study
Exclusion criteria
Exclusion criteria: Obvious infection or pathology in the pelvic area during the treatment process Impossibility of necessary patient cooperation in the treatment process Receiving other treatment at the same time during the sessions of the present study Failure to complete treatment sessions by the patient
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Maximum urine flow(Qmax). Timepoint: Measurement of maximum urine flow before the start of the intervention, 2 weeks and 3 months after the end of the treatment sessions. Method of measurement: Uroflowmetry.;Lower urinary tract symptoms severity. Timepoint: Measurement of lower urinary tract symptoms severity 2 weeks after the end of the treatment sessions. Method of measurement: Persian version of international consultation on incontinence questionnaire – female lower urinary tract symptoms. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyedeh Saeideh Babazadeh
Iran University of Medical Sciences
Outcome results
None listed