Risk Factors for Treatment Failure in Women With Detrusor Overactivity Receiving Combined Pharmacotherapy

NCT07337252 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 61

Last updated 2026-01-13

No results posted yet for this study

Summary

This study evaluated the outcomes of women with detrusor overactivity treated with combined pharmacotherapy to identify risk factors for treatment failure.

Conditions

Interventions

DRUG

Combined pharmacotherapy

Combined pharmacotherapy with oral solifenacin 5 mg and mirabegron 25 mg once daily.

Sponsors & Collaborators

  • Mackay Memorial Hospital

    lead OTHER

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-01
Primary Completion
2024-06-30
Completion
2024-08-31
FDA Drug
Yes

Countries

  • Taiwan

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07337252 on ClinicalTrials.gov