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The investigators will assess the incidence of Overactive Bladder/Detrusor Overactivity (OAB/DO) post-operatively in patients post robotic assisted radical prostatectomy (RARP) and to investigate whether fesoterodine will alter the incidence of OAB/DO in these patients. Additionally, the correlation between OAB symptoms and urodynamic DO will be analyzed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Fesoterodine 4mg | Experimental | Fesoterodine 4mg, Oral once daily for three months |
|
| Placebo | Placebo Comparator | Placebo Oral once daily for three months |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Fesoterodine | Drug | 4 mg |
| |
| Placebo oral tablet |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Adverse Events | 3 months |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| David Lee, MD | Abramson Cancer Center at Penn Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Abramson Cancer Center of the University of Pennsylvania | Philadelphia | Pennsylvania | 19104 | United States |
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| Drug |
Placebo |
|
| ID | Term |
|---|---|
| C526675 | fesoterodine |
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