Comparison of Prostate Fusion Biopsies With Software and Cognitive
Primary Purpose
Prostate Cancer Detection, Fusion Prostate Biopsy
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
cognitive vs software
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Cancer Detection focused on measuring prostate biopsy, mpMRI
Eligibility Criteria
Inclusion Criteria:
- Age over 40 years.
- mpMRI carried out in our center.
- Presence of lesions with PIRADSv.2 ≥ 3.
- Acceptance to participate in the study.
Exclusion Criteria:
- PSA> 30 ng / ml
- Treatment with 5-ARIs (5-alpha-reductase inhibitors).
- Previous diagnosis of PCa.
- TR> T3.
Sites / Locations
- Hospital Vall d'HebronRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
0: cognitive
1: software
Arm Description
target prostate biopsies by cognitive fusion
target prostate biopsies by software
Outcomes
Primary Outcome Measures
Rate of overall prostate cancer and significant prostate cancer between the groups
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed.
Secondary Outcome Measures
Rate of overall prostate cancer and significant prostate cancer between the groups according to the location of the lesions.
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the location of the lesions.
Rate of overall prostate cancer and significant prostate cancer between the groups according to the size of the lesions.
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the size of the lesions.
Rate of overall prostate cancer and significant prostate cancer between the groups according to the PIRADS (prostate imaging and reporting and data System) of the lesions.
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the PIRADS (prostate imaging and reporting and data System) of the lesions.
Rate of overall prostate cancer and significant prostate cancer between the groups according to the prostate volume.
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the prostate volume.
Full Information
NCT ID
NCT04291742
First Posted
February 2, 2020
Last Updated
February 27, 2020
Sponsor
Hospital Universitari Vall d'Hebron Research Institute
1. Study Identification
Unique Protocol Identification Number
NCT04291742
Brief Title
Comparison of Prostate Fusion Biopsies With Software and Cognitive
Official Title
Prospective and Randomized Study to Compare the Efficacy of Cognitive Fusion Prostate Biopsies and Prostate Biopsies Performed by "BK-fusion®" Software, for the Diagnosis of Significant Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 16, 2020 (Actual)
Primary Completion Date
February 27, 2022 (Anticipated)
Study Completion Date
February 27, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital Universitari Vall d'Hebron Research Institute
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This study evaluates the efficacy to diagnose significant prostate cancer in patients with suspicious lesions in mpMRI (multiparametric magnetic resonance imaging) by comparing prostate biopsies performed by cognitive fusion with respect to those performed with software fusion (BK-fusion®). Half of the patients included will undergo a systematic prostate biopsy + target biopsies by cognitive fusion and the other half of the population, will undergo a systematic prostate biopsy + target biopsies by software fusion.
Detailed Description
Various techniques have been developed to perform targeted prostate biopsies aimed at suspicious lesions detected in mpMRI. The two most frequently used are cognitive fusion, in which the physician locates the areas where the mpMRI detects suspicious lesions and directs the puncture by ultrasound; and software fusion, in which the images of the mpMRI are integrated by a software with the ultrasound allowing to direct the puncture to the lesion itself. Both forms of fusion biopsy have proven to be superior to systematized prostate biopsies in the detection of significant prostate cancer, although neither has demonstrated superiority over the other.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer Detection, Fusion Prostate Biopsy
Keywords
prostate biopsy, mpMRI
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
804 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
0: cognitive
Arm Type
Experimental
Arm Description
target prostate biopsies by cognitive fusion
Arm Title
1: software
Arm Type
Experimental
Arm Description
target prostate biopsies by software
Intervention Type
Diagnostic Test
Intervention Name(s)
cognitive vs software
Intervention Description
cognitive vs software
Primary Outcome Measure Information:
Title
Rate of overall prostate cancer and significant prostate cancer between the groups
Description
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Rate of overall prostate cancer and significant prostate cancer between the groups according to the location of the lesions.
Description
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the location of the lesions.
Time Frame
2 years
Title
Rate of overall prostate cancer and significant prostate cancer between the groups according to the size of the lesions.
Description
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the size of the lesions.
Time Frame
2 years
Title
Rate of overall prostate cancer and significant prostate cancer between the groups according to the PIRADS (prostate imaging and reporting and data System) of the lesions.
Description
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the PIRADS (prostate imaging and reporting and data System) of the lesions.
Time Frame
2 years
Title
Rate of overall prostate cancer and significant prostate cancer between the groups according to the prostate volume.
Description
Differences in percentage of detection of overall prostate cancer and prostate cancer ISUP equal or greater than 2 between both groups will be assessed according to the prostate volume.
Time Frame
2 years
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age over 40 years.
mpMRI carried out in our center.
Presence of lesions with PIRADSv.2 ≥ 3.
Acceptance to participate in the study.
Exclusion Criteria:
PSA> 30 ng / ml
Treatment with 5-ARIs (5-alpha-reductase inhibitors).
Previous diagnosis of PCa.
TR> T3.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ana Celma, MD
Phone
0034932746000
Ext
6370
Email
acelma@vhebron.net
First Name & Middle Initial & Last Name or Official Title & Degree
Ignasi Gallardo, Ph
Phone
0034932746000
Ext
6370
Email
ignasi.gallardo@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ana Celma, MD
Organizational Affiliation
Hospital Vall d'Hebron, Barcelona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Vall d'Hebron
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ana Celma, MD
Phone
0034932746000
Ext
6370
Email
acelma@vhebron.net
First Name & Middle Initial & Last Name & Degree
Ignasi Gallardo, Ph
Phone
0034932746000
Ext
6370
Email
ignasi.gallardo@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Comparison of Prostate Fusion Biopsies With Software and Cognitive
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