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临床试验/NCT02450266
NCT02450266Unknown不适用

Prospective Multicenter, Randomized Study Comparing the Diagnostic Efficacy of a Targeted MRI/Ultrasound Fusion-guided Prostate Biopsy Versus a Systematic Transrectal Ultrasound-guided Biopsy in Men With at Least on Negative Prostate Biopsy

Heinrich-Heine University, Duesseldorf6 个研究点 分布在 1 个国家目标入组 586 人开始时间: 2015年2月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
586
试验地点
6
主要终点
Detection rate of significant prostate cancers

研究概览

简要总结

Patients will be submitted to a multiparametric MRI examination of the prostate. Subsequently, all participants will be randomized (1:1) into both study arms. In study arm A patients will be submitted to the gold-standard which comprises systematic transrectal ultrasound-guided prostate biopsy. In study arm B patients will be submitted to targeted prostate biopsy based on the multiparametric MRI findings.

详细描述

In men with previously negative prostate biopsy and persistent elevated prostate-specific antigen (PSA) value, it is unclear which biopsy strategy offers the highest detection rate for significant prostate cancer. The hypothesis of this study is that targeted MRI/ultrasound fusion-guided biopsy improves the detection rates of significant prostate cancers compared with systematic transrectal ultrasound-guided prostate biopsy.

Men with at least one previously negative transrectal ultrasound-guided biopsy and persistently elevated PSA values (> 3 ng/ml) or PSA velocity >0.75 ng/ml/p.a. will be submitted to a multiparametric MRI examination of the prostate. Subsequently, all participants will be randomized (1:1) into both study arms. In study arm A patients will be submitted to the gold-standard which comprises systematic transrectal ultrasound--guided prostate biopsy. In study arm B patients will be submitted to targeted prostate biopsy based on the multiparametric MRI findings. Targeted biopsies will be performed using MRI/ultrasound fusion-guided.

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
Male
接受健康志愿者

入选标准

  • At least one negative transrectal ultrasound-guided prostate biopsy
  • PSA > 3.0 ng/ml or PSA velocity >0.75 ng/ml/p.a.

排除标准

  • Known prostate cancer
  • PSA >50 ng/ml
  • Previous MRI-targeted prostate biopsy

研究组 & 干预措施

A: Transrectal ultrasound-guided biopsy

Active Comparator

Patients of arm A receive a systematic transrectal ultrasound-guided prostate biopsy (12-18 biopsy cores depending on individual prostate volume)

干预措施: Systematic transrectal ultrasound-guided prostate biopsy (Device)

B: MRI/ultrasound fusion-guided biopsy

Experimental

Patients of arm B receive a targeted MRI/ultrasound fusion-guided prostate biopsy. From each prostate lesion defined in the diagnostic multiparametric MRI two targeted biopsy cores will be taken.

干预措施: MRI/ultrasound fusion-guided prostate biopsy (Device)

结局指标

主要结局

Detection rate of significant prostate cancers

时间窗: One week after biopsy

次要结局

  • Overall detection rate of prostate cancers(One week after biopsy)

研究者

发起方
Heinrich-Heine University, Duesseldorf
申办方类型
Other
责任方
Sponsor

研究点 (6)

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