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Clinical Trials/NCT02450266
NCT02450266
Unknown
N/A

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, Duesseldorf3 sites in 1 country586 target enrollmentFebruary 2015
ConditionsProstate Cancer

Overview

Phase
N/A
Intervention
Not specified
Conditions
Prostate Cancer
Sponsor
Heinrich-Heine University, Duesseldorf
Enrollment
586
Locations
3
Primary Endpoint
Detection rate of significant prostate cancers
Last Updated
10 years ago

Overview

Brief Summary

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.

Detailed Description

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.

Registry
clinicaltrials.gov
Start Date
February 2015
End Date
February 2018
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Sponsor
Heinrich-Heine University, Duesseldorf
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

Detection rate of significant prostate cancers

Time Frame: One week after biopsy

Secondary Outcomes

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

Study Sites (3)

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