Actively Recruiting
Robot-Assisted Prostate Biopsy With a Novel Ultrasound Probe
Led by Johns Hopkins University · Updated on 2025-12-08
60
Participants Needed
1
Research Sites
244 weeks
Total Duration
On this page
Sponsors
J
Johns Hopkins University
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Prostate cancer (PCa) is the most diagnosed type of cancer and the second leading cause of cancer related deaths among US men, and its incidence has increased steadily in the last decade. Efforts to address the rise in PCa diagnosis without overdetection and overtreatment include targeted biopsy techniques for clinically significant PCa using magnetic resonance imaging (MRI), and precision targeted biopsy guided by ultrasound and fused to the MRI. The study aims to improve prostate biopsy with a novel ultrasound probe and robot developed at Johns Hopkins, the ProBot device. The trial is a Phase 1 clinical trial to evaluate the safety and feasibility of the new device. ProBot is an entirely new concept including a novel ultrasound probe and robot kinematics specifically designed for the prostate. It operates with only two degrees of freedom configured such that the motions for 3D image scanning and biopsy may not deform the prostate gland, thus improving the accuracy of MRI-ultrasound fusion and needle targeting at biopsy. ProBot is a small and lightweight robot (1.3Kg including the ultrasound probe). It allows hands-free operation of its ultrasound probe at 3D image scanning and needle targeting supervised by the urologist. In addition to MRI-targeted biopsy (TB), at systematic biopsy (SB), instead of using the common template plan that is the same for all patients, the innovative software optimizes the plan for each patient to obtain a diagnosis that is representative of the whole gland histology. The ProBot robot is also uniquely capable of transrectal (TR) and transperineal (TP) biopsy. The aims of the study are to determine the safety and feasibility of the new device at TR and TP biopsies.
CONDITIONS
Official Title
Robot-Assisted Prostate Biopsy With a Novel Ultrasound Probe
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men between the ages of 40 and 75
- Men with one or more high-risk features: PSA > 4.0 ng/ml and/or abnormal digital rectal examination
- Men with atypical small acinar proliferation (ASAP) on previous biopsy
- Men with multiparametric or biparametric MRI exams including PI-RADS 2 or less, and PI-RADS 3 or more
You will not qualify if you...
- Female and children
- Patients without available multiparametric MRI exams
- Patients for whom transrectal or transperineal biopsy is high risk including those with previous rectal surgery, anal stenosis, or coagulopathy
- Patients on active anticoagulation medication (e.g., Coumadin, Lovenox, Heparin)
- Patients unable to tolerate periprostatic Lidocaine block anesthesia or with high anesthesia risk
- Patients who have already had a prostate biopsy using the ProBot device
- Vulnerable populations such as prisoners or institutionalized individuals
- Patients unwilling or unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Johns Hopkins Hospital
Baltimore, Maryland, United States, 21287
Actively Recruiting
Research Team
R
Rana Harb
CONTACT
S
Sara A Naizghi
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DEVICE_FEASIBILITY
Number of Arms
2
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