Actively Recruiting

Phase 1
Age: 40Years - 75Years
MALE
NCT07271017

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

Age: 40Years - 75Years
MALE

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Johns Hopkins Hospital

Baltimore, Maryland, United States, 21287

Actively Recruiting

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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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