Skip to content

Mirabegron combined with behavioral intervention for overactive bladder: a prospective multicenter randomized controlled clinical study

Mirabegron combined with behavioral intervention for overactive bladder: a prospective multicenter randomized controlled clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058592
Enrollment
Unknown
Registered
2022-04-12
Start date
2022-04-12
Completion date
Unknown
Last updated
2024-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Overactive Bladder

Interventions

Experimental group:Mirabegron and behavior intervention
Control group:Mirabegron

Sponsors

Peking Union Medical College Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged 40-60 years, general examination, nervous system examination and pelvic examination showed no abnormality; 2. Patients with symptoms of urgent urination for more than 3 months, with or without urge incontinence, often combined with frequent urination and nocturia, had normal urine routine; 3. For patients diagnosed with OAB through the following questionnaire, scores of 6=12 were considered severe 0AB, and moderate to severe OAB patients were selected into the group; 4. Volunteer and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Other diseases with OAB symptoms; 2. Patients with hypertension, whose blood pressure is up to 180/110 mm Hg or above; 3. Gynecological malignancies, patients after pelvic radiotherapy, patients with stress urinary incontinence and patients with mixed urinary incontinence mainly stress urinary incontinence; 4. Patients taking OAB treatment drugs; 5. Pregnant patients (blood G-HCG must be determined when necessary) or lactating patients; 6. Patients with liver and kidney dysfunction, immunosuppressant treatment, blood diseases, diabetes, mental illness or suffering from other serious diseases; 7. Poor compliance; 8. Allergies or allergies to study medications.

Design outcomes

Primary

MeasureTime frame
Voiding diary;Overactive bladder symptom scale (OABSS);Overactive bladder syndrome questionnaire OAB-Q;Blood pressure;Frequency of urgent urination /24 hours;Urgent incontinence times /24 hours;Frequency of urination /24 hours;The number of nocturnal urination and the maximum urine output;

Countries

China

Contacts

Public ContactShi Honghui
honghuishi@sina.com+86 15711129505

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026