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NCT06094322Completed

Evaluation of Rapid T2-weighted and DWI MR Sequences Reconstructed by Deep Learning for Prostate Imaging

Advanced DL-based T2w and DWI MR Sequences for Prostate Imaging

Source: ClinicalTrials.gov · Last updated 8 Dec 2025

Brief summary (registry, in English)

MR prostate exam is essential for the diagnosis, workup and follow-up of prostate cancer. It allows to detect subclinical prostate cancer following an increase in the level of PSA. The investigators can score the lesion according to the PIRADS classification and obtain an estimate of lesion malignancy. To perform this classification, T2 and DWI sequences are essential. Detection and characterization of malignant lesion is important to address appropriate patient care pathway. The purpose of this project is to evaluate novel deep learning (DL) T2-weighted TSE (T2DL) and Diffusion (DWIDL) sequences for prostate MR exam and investigate its impact on diagnostic, examination time, image quality, and PI-RADS classification compared to standard T2-weighted TSE (T2S) and standard Diffusion (DWIS) sequences.

Status (registry)
Completed
Study type
Interventional
Enrollment
34 (actual)
First submitted
17 Oct 2023
Start date
28 Jul 2022
Primary completion date
9 Apr 2024
Lead sponsor
Centre Hospitalier Universitaire, Amiens
NCT number
NCT06094322

What you commit to

  • Study type: Interventional
  • Participants enrolled: 34
  • From 28 Jul 2022 to the primary completion date, 9 Apr 2024
  • 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.

Other illness

  • History of prostatectomy or irradiation of the prostate

Age

  • Age \< 18 years,

Other

  • claustrophobia,
  • major obesity (\>140 kg),
  • Patient under guardianship or curators
  • Women,
  • any contraindication to MRI exam

Who the study is looking for

  • Age ≥ 18 ans
  • Healthy subject without history of hepatic disease
  • Patient addressed for an prostate MRI
  • Ability to give consent

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Centre Hospitalier Universitaire d'Amiens
Coordinator of this site? Confirm its status
AmiensFranceUnknown status

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