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Clinical Trial to Evaluate Post-Operative Outcomes of Ureteral Stent vs Ureteral Stent Free Radical Cystectomy
NCT07234968 · Thomas Jefferson University
In plain English
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Official title
Randomized Controlled Trial to Evaluate Post-Operative Outcomes of Ureteral Stent vs Ureteral Stent Free Radical Cystectomy
About this study
Patients who are indicated for RCIC will be recruited for this prospective RCT. Ureteral stents will be placed intraoperatively and removed at follow-up visit per surgeon discretion. Either approach would be considered standard of care for muscle invasive bladder cancer, for which radical cystectomy with urinary diversion is the gold standard of treatment.
Patients will be randomized 1:1 to receive stent or no stent during RCIC (Stent: N=35, No Stent: N=35). Randomization will be stratified by surgical approach (open vs. robotic vs. hybrid). The randomization schedule will be created by the study statistician using the method of random permuted blocks.
Stent placement, if applicable, will be a one-time occurrence inserted during RCIC, and be removed typically between 7-21 days post-op at the discretion of the surgeon. For this study, subjects will continue to be followed for up to 1-year post-op. Subjects will be enrolled in this study for 12 months.
Post treatment, the patient will have a follow-up visit within 30 days post-operatively, 3 months follow-up visit (+/- 1 week), 6 months follow-up visit (+/- 21 days), and 12 months follow-up visit (+/- 21 days). Patient will be followed for 12 months post treatment or until their death. Additional visits or follow-ups may be indicated for instances of the need for replacement of ureteral stents and catheters or percutaneous nephrostomies. The need for surgical repair for a ureteral leak or stricture may also occur.
The Principal Investigator hypothesizes that patients with no ureteral stent placement during RCIC will not be associated with a higher risk of post-op complications compared to those with a ureteral stent.
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 to 85
* Diagnosed with bladder cancer, other pelvic malignancies necessitating a cystectomy (e.g.: colorectal, prostate, gynecologic) and have elected for a cystectomy with ileal conduit urinary diversion
Exclusion Criteria:
* An individual who meets any of the following criteria will be excluded from participation in this study:
* Current or history of pelvic radiation
* Retroperitoneal fibrosis
* Untreated urinary tract infection (UTI) within 30 days prior to RCIC
* Pregnancy
Study design
Enrollment target: 70 participants
Allocation: randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2025-12-23
Estimated completion: 2028-04-30
Last updated: 2026-02-17
Interventions
Procedure: Ureteral Stent PlacementProcedure: No Ureteral StentDiagnostic Test: Indocyanine Green with Fluorescence Imaging
Primary outcomes
- • Number of urinary tract infection (UTI) (90 days after surgery)
Sponsor
Thomas Jefferson University · other
Contacts & investigators
ContactMihir S Shah, MD · contact · Mihir.Shah@jefferson.edu · 215-955-6961
InvestigatorMihir S Shah, MD · principal_investigator, Thomas Jefferson University
All locations (2)
Thomas Jefferson University HospitalRecruiting
Philadelphia, Pennsylvania, United States
Jefferson Einstein Philadelphia HospitalNot Yet Recruiting
Philadelphia, Pennsylvania, United States