跳至主要内容
临床试验/NCT00318266
NCT00318266已完成不适用

NMP22 Provides Improved Sensitivity in Detecting Bladder Cancers

Lawson Health Research Institute1 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
73
试验地点
1

研究概览

简要总结

It is hypothesized that the NMP22(Nuclear Matrix Protein) Bladder Check ® Test will demonstrate improved sensitivity over that of standard urine cytology for patients with superficial transitional cell carcinoma at high risk of recurrence.

详细描述

Patients who have been previously treated for bladder cancer and are at a high risk for recurrence are being monitored for recurrence every 3 months with urine cytology and cystoscopy as part of standard care.The NMP22 Bladder Cancer ® Test Kit has been designed to provide an alternative to regular urine cytology. A urine sample will be provided and divided with a portion being used to assess the NMP22 test kit and the remaining sample to be sent to the lab for regular urine cytology. Patient charts will be reviewed by a medical student to record age, clinical stage, pathologic stage, time to disease progression/recurrence, site of recurrence and survival data.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • · History of pTis, pT1, large (>2cm) pTa or multiple pTa bladder cancer tumours.
  • Written Informed Consent prior to any study-related procedures.

排除标准

  • History of bladder cancer tumours other than those listed in inclusion

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验

NMP22 Provides Improved Sensitivity in Detecting... | 临床试验