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Tests an AI tool with ultrasound and contrast to detect prostate cancer

Tests an AI ultrasound method for finding significant prostate cancer in adult men.

Plain-language title generated from the registry record
Registry title: TULIP ReTrain Study

Key facts

Where
Amsterdam, NetherlandsSee the site

Where in Netherlands

  • Amsterdam UMCAmsterdam, NetherlandsNo longer taking part

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Trial details

Who runs it
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Trial code
NCT06974539
Record updated
16 May 2025
Original description
This prospective clinical study aims to retrain and validate the PCaVision AI algorithm for the detection and localization of clinically significant prostate cancer (csPCa) using multiparametric ultrasound (mpUS) with two different ultrasound contrast agents: Sonovue and Optison. Data will be collected using a commercial version of the LOGIQ E10 ultrasound machine, with full histopathological correlation in patients undergoing radical prostatectomy.Read full original descriptionShow less

Optimization of PCaVision: A Prospective Study for CAD-based Detection of Clinically Significant Prostate Cancer Using mpUS and Contrast Agents

This prospective clinical study aims to retrain and validate the PCaVision AI algorithm for the detection and localization of clinically significant prostate cancer (csPCa) using multiparametric ultrasound (mpUS) with two different ultrasound contrast agents: Sonovue and Optison. Data will be collected using a commercial version of the LOGIQ E10 ultrasound machine, with full histopathological correlation in patients undergoing radical prostatectomy.

Inclusion: Male ≥18 years; Cohort 1: Histologically confirmed prostate cancer scheduled for radical prostatectomy; Cohort 2: Negative multiparametric prostate MRI (PI-RADS ≤ 2).

Exclusion: Severe pulmonary hypertension; Cardiac right-to-left shunt; Known allergy to Sonovue or Optison; Contraindication for ultrasound contrast agents.

ClinicalTrials.gov NCT06974539