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临床试验/NCT00785694
NCT00785694撤回4 期

Recurrence of Bladder Cancer After Transurethral Resection With Hexvix

GE Healthcare1 个研究点 分布在 1 个国家开始时间: 2008年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
撤回
发起方
GE Healthcare
试验地点
1
主要终点
Rate of bladder cancer recurrence

研究概览

简要总结

This is a randomised, comparative, multicentre study to determine if the early recurrence rate of intermediate-risk bladder cancer is similar in subjects treated with multiple instillations of mitomycin C after resection conducted under white light cystoscopy (group A) and subjects treated with 1 instillation of mitomycin C after resection conducted under white light and blue light cystoscopy (group B).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Diagnostic
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

  • The subject is not of childbearing potential and signed informed consent.
  • Subject with 1 or more primary bladder tumours, confirmed on an outpatient cystoscopy or subjects with 1 or more recurrent bladder tumours appearing within 12 months of removal of a previous bladder tumour, confirmed on an outpatient cystoscopy.

排除标准

  • The subject was previously included in this study.
  • The subject has a history/is suspected to have TaG3 or greater than or equal to T1 tumours or carcinoma in situ (CIS).
  • The subject is suspected to have single primary or single recurrent TaG1 tumours when recurrence occurs more than 1 year after initial diagnosis or previous recurrence.
  • The subject has known tumours in the prostatic urethra, distal urethra, or upper urinary tract.
  • The subject has gross haematuria.
  • The subject has a history of porphyria.

研究组 & 干预措施

B

Experimental

One instillation of mitomycin C after transurethral resection in white and blue fluorescence light with Hexvix.

干预措施: hexaminolevulinate (Drug)

结局指标

主要结局

Rate of bladder cancer recurrence

时间窗: 12 Months

次要结局

未报告次要终点

研究者

发起方
GE Healthcare
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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