Clinical Trial to Evaluate Post-Operative Outcomes of Ureteral Stent vs Ureteral Stent Free Radical Cystectomy
Recruiting
N/A
Interventional Study
Bladder Cancer
Muscle-Invasive Bladder Carcinoma
Urothelial Carcinoma
Pelvic Malignancy
Bladder Transitional Cell Carcinoma
Bladder Neoplasm
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 85
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 70 (estimated)
- Sponsor
- Thomas Jefferson University · Other
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About This Trial
Subjects will be randomized into 2 groups (stent or no stent) prior to radical cystectomy with ileal conduit urinary diversion (RCIC). They will follow the standard of care and be enrolled in the study for 12 months post-op. Risk of post-op complications will be analyzed.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Individuals must meet all the following inclusion criteria to be eligible to participate in the study:
* Provide signed and dated informed consent form
* Willing to comply with all study procedures and be available for the duration of the study
* Male or female, age 18 …
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