Ireland
--:--IST
Starting soon Observational

CascadeDiagnose Prostate MRI

NCT07844304 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2026-10-01
Last updated
2026-09-28

Condition(s) studied

Prostate Cancer (Diagnosis)

Study summary

This multicenter clinical study is evaluating CascadeDiagnose Prostate MRI, an artificial-intelligence software tool that analyzes standard prostate MRI scans-T2-weighted, diffusion-weighted, and ADC images-to help radiologists detect suspicious prostate lesions, estimate cancer risk, and distinguish prostate cancer from benign conditions. The study will take place at six hospitals in Guangxi and plans to enroll at least 2,000 eligible men aged 18 or older who have had prostate MRI and have confirmed pathology results. It includes a retrospective phase using existing records and a prospective phase in which participants provide written informed consent. The main goals are to measure the system's diagnostic accuracy (AUC, sensitivity, and specificity), compare it with readings by radiologists, assess safety and rates of rejected or indeterminate results, and see whether it improves reading efficiency or helps reduce unnecessary biopsies. To protect patient privacy, raw MRI, medical-record, and pathology data remain inside each hospital; only de-identified, encrypted intermediate results are shared through a secure distributed network. The study requires ethics approval and trial registration before enrollment, and its results may help determine whether this AI tool is safe and effective for clinical use.

Eligibility

Sex
MALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Male patients aged ≥ 18 years undergoing prostate MRI examination. 2. Complete MRI sequences including at minimum T2WI, DWI, and ADC sequences. 3. Definitive pathological diagnosis (prostate biopsy or post-surgical pathology) with complete Gleason-score information. 4. Complete clinical data including serum PSA level, age, and prior medical history. 5. Patient informed consent (written informed consent required for the prospective phase). Exclusion Criteria: 1. Substantial MRI image degradation caused by motion artifacts or metal artifacts that severely impair interpretation. 2. Prior prostate biopsy, prostate surgery, radiotherapy, or endocrine therapy. 3. Medical history of other malignant neoplasms. 4. Missing key MRI data or reference-standard materials required for primary-endpoint evaluation, precluding assessment of primary study outcomes. 5. Severe systemic diseases (e.g., heart failure, end-stage renal disease) interfering with imaging assessment or prognostic evaluation.

Primary outcome measure(s)

  • Adverse Events — up to 24 weeks
    All adverse events associated with system usage are documented
  • Area under the receiver operating characteristic curve (AUC) — up to 24 weeks
    overall diagnostic performance for discriminating prostate cancer from benign lesions

Trial sites (6)

FacilityCityRegionStatus
Guigang People's Hospital Guigang Guangxi
Guilin People's Hospital Guilin Guangxi
Liuzhou People's Hospital Liuzhou Guangxi
The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi
The Second People's Hospital of Nanning Nanning Guangxi
Wuzhou Red Cross Hospital Wuzhou Guangxi
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07844304 on ClinicalTrials.gov ↗ ← All trials in China