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NCT06183905Active, not recruiting

Multi-parametric Ultrasound Versus Multi-parametric MRI for Prostate Cancer Detection

A Prospective Cohort Study Comparing Multi-parametric Ultrasound Versus Multi-parametric MRI for Clinically Significant Prostate Cancer Detection

Source: ClinicalTrials.gov · Last updated 21 Jul 2026

Brief summary (registry, in English)

The goal of this cohort study is to investigate multiparametric ultrasound versus multiparametric MRI for clinically significant prostate cancer detection in patients scheduled for initial biopsy. The main questions it aims to answer are: * whether the clinically significant prostate cancer detection rate of multiparametric ultrasound is comparable to multiparametric MRI * the any cancer detection of multiparametric ultrasound versus multiparametric MRI Participants will undergo multiparametric ultrasound and multiparametric MRI before prostate biopsy. In case of suspicious findings on ultrasound or MRI, they will undergo combined systematic biopsy and targeted biopsy. In case of nonsuspicious imaging finding, they will undergo systematic biopsy alone.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
635 (actual)
First submitted
23 Nov 2023
Start date
29 Dec 2023
Primary completion date
30 Jun 2025
Lead sponsor
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
NCT number
NCT06183905

What you commit to

  • Study type: Interventional
  • Participants enrolled: 635
  • From 29 Dec 2023 to the primary completion date, 30 Jun 2025
  • 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

  • Contraindications to MRI, such as metal implants, claustrophobia, etc;

Other illness

  • Contraindications to ultrasound, such as acute myocardial infarction, acute cerebral infarction and rectal tumor after Miles operation;
  • Any medical condition or other event that may significantly reduce the chances of obtaining reliable data, achieving the purpose of the study or completing the study and follow-up;

Other

  • Contraindications of prostate biopsy, such as abnormal routine urine test, coagulation function and electrocardiogram
  • The study doctor thinks it is not suitable to participate in this study.

Who the study is looking for

  • Scheduled for prostate biopsy;
  • Signed the informed consent.

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
Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status

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