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| ID | Type | Description | Link |
|---|---|---|---|
| NCI-2014-01530 | Registry Identifier | CTRP (Clinical Trial Reporting Program) | |
| CASE 7814 | Other Identifier | Case Comprehensive Cancer Center | |
| P30CA043703 | U.S. NIH Grant/Contract | View source |
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waiting on surgeon training
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| Name | Class |
|---|---|
| National Cancer Institute (NCI) | NIH |
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This randomized clinical trial studies intracorporeal or extracorporeal urinary diversion during robotic assisted radical cystectomy in reducing complications in patients with bladder cancer. Radical cystectomy is surgery to remove the entire bladder as well as nearby tissues and organs. After the bladder is removed, urinary diversion (a surgical procedure to make a new way for urine to leave the body) is performed. It is not yet known whether intracorporeal (within the body) or extracorporeal (outside of the body) urinary diversion is a better method in patients with bladder cancer undergoing robotic assisted radical cystectomy.
PRIMARY OBJECTIVES:
I. To compare perioperative outcomes and complications after robotic assisted radical cystectomy (RARC) with intracorporeal urinary diversion (IUD) and RARC with extracorporeal urinary diversion (EUD) in a prospective randomized fashion.
SECONDARY OBJECTIVES:
I. Time to passage of flatus. II. Analgesic requirement (narcotic use). III. Hospital length of stay. IV. Total operating time. V. Estimated blood loss. VI. Readmission rate. VII. Bladder Cancer Index Questionnaire. VIII. Ureteral strictures. IX. Stomal stenosis. X. Disease recurrence. XI. Secondary procedures.
OUTLINE: Patients are randomized to 1 of 2 treatment arms.
ARM I: Patients undergo RARC with IUD.
ARM II: Patients undergo RARC with EUD.
After completion of study treatment, patients are followed up within 90 days and then for 2-5 years.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm I (RARC with IUD) | Experimental | Patients undergo RARC with IUD. |
|
| Arm II (RARC with EUD) | Experimental | Patients undergo RARC with EUD. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| robot-assisted laparoscopic surgery | Procedure | Undergo RARC with IUD |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Complication rate | Analyzed using multivariable logistical regression. Descriptions and grading scales found in the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 will be utilized for adverse event reporting. | 90 days after surgery |
| Measure | Description | Time Frame |
|---|---|---|
| Time to passage of flatus | Analyzed using regression analysis. | Up to 90 days |
| Analgesic requirement (narcotic use) | Analyzed using logistical regression. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Jihad Kaouk | Case Comprehensive Cancer Center | Principal Investigator |
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| robot-assisted laparoscopic surgery |
| Procedure |
Undergo RARC with EUD |
|
| intraoperative complication management/prevention | Other | Undergo RARC with IUD |
|
| intraoperative complication management/prevention | Other | Undergo RARC with EUD |
|
| quality-of-life assessment | Other | Ancillary studies |
|
|
| Up to 90 days |
| Hospital length of stay | Analyzed using regression analysis. | Up to 90 days |
| Total operating time | Analyzed using regression analysis. | Up to completion of surgery |
| Estimated blood loss | Analyzed using regression analysis. | Up to 90 days |
| Readmission rate | Analyzed using regression analysis. | Up to 90 days |
| Quality of life assessed using the Bladder Cancer Index Questionnaire | The Cox proportional hazards model will be used. The hazard ratio (HR) and 95% confidence interval (95% CI) associated with the use of RARC with IUD compared with the use of RARC with EUD will be calculated. | Up to 5 years |
| Ureteral strictures | The Cox proportional hazards model will be used. The HR and 95% CI associated with the use of RARC with IUD compared with the use of RARC with EUD will be calculated. | Up to 5 years |
| Stromal stenosis | The Cox proportional hazards model will be used. The HR and 95% CI associated with the use of RARC with IUD compared with the use of RARC with EUD will be calculated. | Up to 5 years |
| Disease recurrence | The Cox proportional hazards model will be used. The HR and 95% CI associated with the use of RARC with IUD compared with the use of RARC with EUD will be calculated. | Up to 5 years |
| Secondary procedures | The Cox proportional hazards model will be used. The HR and 95% CI associated with the use of RARC with IUD compared with the use of RARC with EUD will be calculated. | Up to 5 years |
| Cumulative complication incidence | Graphically described using the Kaplan-Meier method. Descriptions and grading scales found in the NCI CTCAE version 4.0 will be utilized for adverse event reporting. | Up to 5 years |
| ID | Term |
|---|---|
| D001749 | Urinary Bladder Neoplasms |
| ID | Term |
|---|---|
| D014571 | Urologic Neoplasms |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D001745 | Urinary Bladder Diseases |
| D014570 | Urologic Diseases |
| D052801 | Male Urogenital Diseases |
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