A Prospective, Observational, Multicenter Study of Patients Following Initiation of a New Course of Treatment for Overactive Bladder (OAB)
Status: | Completed |
---|---|
Conditions: | Overactive Bladder, Urology |
Therapuetic Areas: | Gastroenterology, Nephrology / Urology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/24/2018 |
Start Date: | January 5, 2015 |
End Date: | August 4, 2017 |
A Prospective, Non-interventional, Registry Study of Patients Initiating a Course of DrugTherapy for Overactive Bladder (OAB)
A study to identify factors that are associated with improved effectiveness in pharmacologic
therapy of Overactive Bladder, from the patient perspective primarily measured by OAB-Q-SF
(Overactive Bladder Questionnaire Short Form)
therapy of Overactive Bladder, from the patient perspective primarily measured by OAB-Q-SF
(Overactive Bladder Questionnaire Short Form)
Inclusion Criteria:
- Diagnosed with OAB (with or without urgency incontinence) by the treating HCP, with
symptoms for at least three months prior to study enrollment
- Initiating a new course of treatment with mirabegron or antimuscarinic medication
(including patch formulation) for OAB, which may be first course of any treatment for
OAB, restart or switch from one drug to another
- Willing and able to complete PRO questionnaires with minimal assistance
Exclusion Criteria:
- Current participation in clinical trials of OAB
- Use of more than one OAB medication at time of enrollment
- Patients whose OAB has been treated with onabotulinumtoxinA, sacral neuromodulation,
percutaneous tibial nerve stimulation, external beam radiation (XRT), stents, surgery,
or intermittent catheterization prior to or at time of enrollment
- Neurologic conditions associated with OAB symptoms
- Patients residing in a nursing home
We found this trial at
76
sites
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