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UnknownNCT05452434

Mirabegron Combined With Behavioral Intervention for Overactive Bladder:a Prospective Multicenter Randomized Controlled Clinical Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
600 (estimated)
Sponsor
Peking Union Medical College Hospital · Academic / Other
Sex
Female
Age
40 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study was to assess the efficacy, safety and tolerability of Mirabegron and behavioral combination versus Mirabegron alone in the treatment of women with overactive bladder (OAB).

Conditions

Interventions

TypeNameDescription
DRUGmirabegronmirabegron 50mg QD for 12 weeks.

Timeline

Start date
2022-07-15
Primary completion
2023-07-15
Completion
2023-07-15
First posted
2022-07-11
Last updated
2022-07-11

Source: ClinicalTrials.gov record NCT05452434. Inclusion in this directory is not an endorsement.

Mirabegron Combined With Behavioral Intervention for Overactive Bladder:a Prospective Multicenter Randomized Controlled (NCT05452434) · Clinical Trials Directory