Female patients complaining of symptoms of overactive bladder syndrome Urological and Genital Diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Female patients 2. Aged over 18 years 3. Complaining of symptoms of overactive bladder syndrome (urgent urination—at least once a day, frequency of urination—more than 8 times per day, nocturia—more than once per night) with or without urgency urinary incontinence for at least 6 months 4. Not having received treatment with antimuscarinic medications for at least 2 weeks before the study start 5. No diagnosis of painful bladder syndrome 6. Bladder volume greater than 150 ml 7. Sufficiently informed and provided written consent for the use of research data 8. Adequate understanding of the Ukrainian language and ability to complete questionnaires 9. Not participating in any other clinical trials simultaneously
Exclusion criteria
Exclusion criteria: 1. The use of antimuscarinics or other medications affecting bladder activity within one month prior to entering the study 2. Participation in another OAB study 3. Painful bladder syndrome, known neurological disorders (e.g., paraplegia, multiple sclerosis, Parkinson’s disease, history of stroke) 4. Stress urinary incontinence (SUI), 5. Active urinary tract infection, confirmed through urine microscopy 6. Infravesical obstruction, grade II or higher vaginal prolapse, or obstructive voiding patterns
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Trospium chloride effect is measured using the Overactive Bladder Symptoms Score and Overactive Bladder Symptoms Bother at baseline and 6 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| Cognitive function is measured using the Montreal Cognitive Assessment (MoCA) at baseline and 6 weeks | — |
Countries
Ukraine