University of Southern California
USC/Norris Comprehensive Cancer Center
If you are a patient, please contact The Doctors of USC at 800-USC-CARE.

Details for trial 4B-01-2


 
Description: A Randomized Comparison of the Studer Pouch vs. the T-Pouch Orthotopic Neobladder Urinary Diversion in Bladder Cancer Patients.
Status: Open
Randomized? Yes


Researchers  
Principal InvestigatorTitle
Eila SkinnerM.D.

Data Management
NameTitle


You may participate in this study if:
 Requirement
1Diagnosed with primary bladder cancer (any histology) who are undergoing radical cystectomy (cystoprostatectomy in men and anterior exenteration in women).
2Felt by the treating MD to be a candidate for an orthotopic neobladder urinary diversion.
3May have received previous RT or intravesical or systemic chemotherapy. If the treatment was for another malignancy, then at least 5 years must have elapsed since the last evidence of disease. Patients with documented metastatic disease are not excluded as long as they are felt to be candidates for a continent neobladder urinary diversion.
4Signed informed consent.


You may not participate in this study if:
1Undergoing radical cystectomy for any malignancy other than primary bladder cancer (e.g., prostate or colon cancer invading the bladder, or a gynecologic malignancy), or non-malignant disease (i.e., neurogenic bladder or radiation cystitis).
2Not eligible for an orthotopic neobladder re-construction.
3History of other malignancy (except skin cancer) within the previous 5 years.


For further information on, or to sign up for this study, please contact the Clinical Investigation Support Office at (323) 865-0451 or the Principal Investigator noted above.