Unspecified urinary incontinence
Conditions
Interventions
This is a randomized clinical study with two arms. After signing the informed consent form, the patients will be randomized into LASER (L) or SHAM (S) groups. The randomization was performed using a c
Sponsors
Univesidade Federal de São Paulo
Univesidade Federal de São Paulo
Eligibility
Sex/Gender
Female
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Women diagnosed clinically with Overactive Bladder Syndrome; Age between 18 and 80 years; Signature of the consent form; A 3-day voiding diary showing 8 or more voids in 24 hours and at least 1 episode of urinary urgency.
Exclusion criteria
Exclusion criteria: Untreated urinary infection; untreated genital infection; Bladder Pain Syndrome; Neurogenic bladder; Stroke, neurological or neurodegenerative diseases; Genital prolapse of any compartment above the hymenal ring; Urinary tract lithiasis or tumors; Physiotherapeutic or drug treatment for SBH within the past 2 months.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Decrease in the number of daily voids by 3.5 in the LASER group and 2 in the SHAM group. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secundary outcomes are expected. | — |
Countries
Brazil
Contacts
Public ContactLuiza Morais
Univesidade Federal de São Paulo
Outcome results
None listed