跳至主要内容
临床试验/NCT07655284
NCT07655284撤回3 期

STENT X Non-stent Genito-urinary Tract Reconstruction After Radical Cystectomy for Bladder Cancer - a Prospective, Randomized, Controlled and Multi Institutional Trial

Brigham and Women's Hospital2 个研究点 分布在 2 个国家目标入组 190 人开始时间: 2026年9月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
撤回
入组人数
190
试验地点
2

研究概览

简要总结

Radical Cystectomy (RC) remains the gold standard for localized muscle-invasive bladder cancer (MIBC); however, use of ureteral stents at time of surgery remains controversial without level 1 evidence to comment on risks or benefits of their use. RC complications commonly include urinary tract infections (UTIs), pyelonephritis, ureteroileal leakage and stenosis, and can occur with either ileal conduit or orthotopic neobladder diversions. Traditionally, ureteral stents are thought to support anastomotic healing and reduce the risk of anastomotic leakage and strictures; however, emerging evidence from retrospective studies suggests that stent use may paradoxically increase rates of postoperative morbidity. This randomized, multicenter and prospective study aims to compare 30-day postoperative complication rates between stented and non-stented urinary diversions in patients undergoing RC for MIBC, in both ileal conduit or neobladder with either robotic or open approaches.

详细描述

Radical Cystectomy (RC) remains the gold standard for localized muscle-invasive bladder cancer (MIBC); however, use of ureteral stents at time of surgery remains controversial without level 1 evidence to comment on risks or benefits of their use. RC complications commonly include urinary tract infections (UTIs), pyelonephritis, ureteroileal leakage and stenosis, and can occur with either ileal conduit or orthotopic neobladder diversions. Traditionally, ureteral stents are thought to support anastomotic healing and reduce the risk of anastomotic leakage and strictures; however, emerging evidence from retrospective studies suggests that stent use may paradoxically increase rates of postoperative morbidity. This randomized, multicenter and prospective study aims to compare 30-day postoperative complication rates between stented and non-stented urinary diversions in patients undergoing RC for MIBC, in both ileal conduit or neobladder with either robotic or open approaches. Randomization between ureteroenteric anastomosis with or without ureteral stent placement will occur at time of surgery; the surgeon will know this information at time of surgery and the patient will be aware of the placement of stents following surgery as these are externalized and visible. The primary outcome will be complication rate in 30 days after the surgery. Secondary outcomes of this trial will include: length of stay, procedure duration, emergency room visits, patient reported pain, anastomotic leakage rate, ureteral stricture rate, post-operative nephrostomy tube placement, differences in complication rates between interrupted and running suture technique. The study will be conducted across three academic institutions: Brigham and Women's Hospital (BWH), Massachusetts General Hospital (MGH) and Instituto do Câncer do Estado de São Paulo (ICESP), Brazil.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults (> 18 years old)
  • Muscle invasive bladder cancer or non-muscle invasive bladder cancer with indication of Radical Cystectomy
  • No concomitant surgeries like nephrectomies, colectomies or removal of other organs affected by the tumor (Except standard lymph node dissections as well as in men the prostate and seminal vesicles and in women the uterus, fallopian tubes, ovaries and vagina, that are considered part of the oncological radical cystectomy.)
  • Patients who have the capacity to understand the study procedures and provide written informed consent

排除标准

  • Simultaneous surgical procedures (except those specified in the inclusion criteria that are considered part of a routine radical cystectomy)
  • History of prior urinary diversion
  • Patients who decline to participate, lack understanding of the study's purpose, or are unable to provide informed consent
  • Cystectomy for other reasons than Bladder cancer
  • Previous radiation therapy in the pelvis for any reason
  • Extremely debilitated patients, malnourished individuals, or those undergoing palliative or hygienic cystectomy

研究组 & 干预措施

ureteral stents placed at time of cystectomy

Active Comparator

standard of care ureteral stent placement at time of radical cystectomy (control arm)

干预措施: ureteral stents (Device)

stent-free, no stent placement at time of cystectomy

Experimental

forgo ureteral stent placement at time of radical cystectomy (intervention arm)

干预措施: no ureteral stent (Device)

结局指标

主要结局

未指定

次要结局

  • patient reported pain on analog scale(30 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Timothy Clinton

Associate Surgeon

Brigham and Women's Hospital

研究点 (2)

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