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Comparing the efficacy of Mirabegron in reducing urinary symptoms associated with cerebrovascular accidents

Comparison of treatment efficacy of Mirabegron with alpha-blockers versus Mirabegron alone in patients of Cerebrovascular accident with lower urinary tract symptoms: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/03/050511
Enrollment
210
Registered
2023-03-09
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: I69- Sequelae of cerebrovascular disease

Interventions

Intervention1: MIRABEGRON GROUP: Medication in the form of (Behavioral therapy + Mirabegron alone) will be given to patients of cerebrovascular accident with lower urinary tract symptoms for 3 months

Sponsors

DEPARTMENT OF UROLOGY KASTURBA MEDICAL COLLEGE MANIPAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All patients with Cerebrovascular accident having moderate/bothersome LUTS as per IPSS questionnaire

Exclusion criteria

Exclusion criteria: Patients with: 1. Montreal Cognitive Assessment score 2. Poorly controlled diabetes or poorly controlled hypertension, 3. Indwelling catheter, 4. Renal dialysis 5. Cardiac failure requiring diuretics 6. Urinary tract infection at presentation 7. Prostate or bladder cancer 8. Uncontrolled bladder outlet obstruction

Design outcomes

Primary

MeasureTime frame
Primary Outcome measures: Change in the objectively measurable parameters namely: 1. Change in day time urinary frequency 2. Change in number of nocturia episodes 3. Change in functional bladder capacity 4. Change in QmaxTimepoint: 4 weeks

Secondary

MeasureTime frame
Change in the 1. IPSS score 2. OABSS (Over Active Bladder Symptom Score) 3. OAB-q SF Score 4. Patient Perception of Bladder Condition (PPBC) 5. OAB family impact measure (OAB-FIM) score Timepoint: 4 WEEKS, 8 WEEKS AND 12 WEEKS

Countries

India

Contacts

Public ContactAnshuman Singh

KASTURBA MEDICAL COLLEGE, MANIPAL

dr.anshumansingh@yahoo.com

Outcome results

None listed

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