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临床试验/ISRCTN13889738
ISRCTN13889738已完成未知

Bladder Cancer Prognosis Programme (incorporating SELENIB trial)

niversity of Birmingham (United Kingdom)0 个研究点目标入组 270 人开始时间: 2006年5月24日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
270

研究概览

简要总结

2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37847504/ (added 23/10/2023)

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • Inclusion criteria for SELENIB Trial:
  • 1. Able to give informed consent for SELENIB
  • 2. Previously registered onto the Bladder Cancer Prognosis Programme
  • 3. Disease characteristics: histopathologically confirmed non-muscle invasive transitional cell carcinoma. Solitary grade 1 pTa larger than 3 cm and all other stage pTa, pT1 or pTcis

排除标准

  • Exclusion criteria for SELENIB trial:
  • 1. Disease characteristics - solitary grade 1 pTa <3 cm or stage pT2 and above
  • 2. Patients that are pregnant or breastfeeding
  • 3. Patients diagnosed with human immunodeficiency virus (HIV) infection
  • 4. Patients who are on immunosuppressive therapy following organ transplantion
  • 5. Patients taking cyclosporin
  • 6. Any condition, which, in the opinion of the local investigator, might interfere with the safety of the patient or evaluation of the trial objectives

研究者

发起方
niversity of Birmingham (United Kingdom)

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