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This study is being done to test the feasibility and accuracy of using an ultrasound-guided core needle biopsy technique as a potential tool for staging urothelial carcinoma of the bladder (UCB).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Observational | Patients undergo standard of care radical cystectomy and residual tissues collected undergo US core needle biopsy. Additionally, patients have their medical records reviewed on study. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Non-Interventional Study | Other | Non-interventional study |
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| Measure | Description | Time Frame |
|---|---|---|
| Concordance between US and core needle biopsy stage and final surgical specimen pathologic stage | The radiology-assessed tumor stage from the ultrasound (US) and the core needle biopsy-assessed tumor stage will be compared with the final pathologic tumor stage. | Baseline (after completion of bladder surgery) |
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Inclusion Criteria:
Exclusion Criteria:
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Patients undergoing radical cystectomy for confirmed or suspected urothelial carcinoma of the bladder
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Hosanna Yeadon, BA | Contact | 507-538-5019 | biffert.hosanna@mayo.edu | |
| Clinical Trials Referral Office | Contact | 855-776-0015 | mayocliniccancerstudies@mayo.edu |
| Name | Affiliation | Role |
|---|---|---|
| Vidit Sharma, MD | Mayo Clinic in Rochester | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic in Rochester | Recruiting | Rochester | Minnesota | 55905 | United States |
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| Label | URL |
|---|---|
| Mayo Clinic Clinical Trials | View source |
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Bladder tissue