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NCT04420702Recruiting

Diffusion Basis Spectrum Imaging of the Prostate

Diffusion Basis Spectrum Imaging of the Prostate: A Virtual Biopsy to Accurately Diagnose Prostate Cancer

Source: ClinicalTrials.gov · Last updated 14 Jul 2026

Brief summary (registry, in English)

Diffusion Basis Spectrum Imaging (DBSI) represents a potential leap forward in improving prostate cancer early detection: a non-invasive and accurate imaging test for clinically significant prostate cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
500 (estimated)
First submitted
3 Jun 2020
Start date
27 Feb 2020
Primary completion date
31 May 2027
Lead sponsor
Washington University School of Medicine
NCT number
NCT04420702

What you commit to

  • Study type: Interventional
  • Planned participants: 500
  • From 27 Feb 2020 to the primary completion date, 31 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients with any clinical contraindication to MRI
    • \*Including but not limited to:
    • Those with metallic implants, such as pacemakers or implantable cardioverter-defibrillators
    • Those with cochlear implants
    • Those with claustrophobia not relieved with medications (patients with claustrophobia who do not need medications for the scan or whose claustrophobia can be managed with medication, are eligible to participate)
    • Those who cannot lie flat for over 1 hour
  • Patients with prior prostate surgery for prostate cancer (e.g. radical prostatectomy, focal ablation)

Who the study is looking for

  • Over 18 years of age and willing and able to provide informed consent.
  • Patients with no prior diagnosis of prostate cancer, who are planning to undergo prostate biopsy as clinical standard of care ("early detection cohort")
  • Including those men with:
    • an elevated PSA and no prior biopsy
    • an elevated PSA and a negative prior biopsy
  • Patients with a prior diagnosis of prostate cancer, who are currently managed with active surveillance, who are planning to undergo biopsy as clinical standard of care ("active surveillance cohort")

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Washington University School of Medicine
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.