Fact CheckerSign in

NCT07112599Recruiting

Study of Predicting Lymph Node Metastasis of High-risk Prostate Cancer by Artificial Intelligence Multi-omics Analysis

Clinical Study on Predicting Lymph Node Metastasis of High-risk Prostate Cancer Based on Artificial Intelligence Multi-omics Analysis:A Multicenter, Prospective and Observational Clinical Study

Source: ClinicalTrials.gov · Last updated 9 Jan 2026

Brief summary (registry, in English)

The pathological-omics and imaging-omics in this study are combined to construct an artificial intelligence (AI) model that can predict whether high-risk prostate cancer patients may have lymph node metastasis. The model determines whether the patient has lymph node metastasis based on the MRI results and the pathological section image information of the case combined with clinical data before radical resection of the prostate. This study is a multicenter, prospective clinical study to verify the model's ability to predict whether high-risk prostate cancer patients may have lymph node metastasis.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
28 Jul 2025
Start date
25 Jan 2026
Primary completion date
30 Dec 2026
Lead sponsor
Anhui Medical University
NCT number
NCT07112599

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 25 Jan 2026 to the primary completion date, 30 Dec 2026
  • 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 contraindications to MRI examination, such as metal implants in the body, claustrophobia, etc.

Other illness

  • Patients with a clear history of neurological and psychiatric disorders, such as dementia, epilepsy, or seizures

Lab values

  • In the judgment of the investigator, there are serious concomitant diseases that endanger the safety of the subjects or affect the subjects' completion of this study (such as severe diabetes, thyroid disease, and mental illness, etc.), or factors that affect the safety of the patients or affect the patients' provision of informed consent (including laboratory abnormalities), or any psychological, family, sociological or geographical conditions that affect the study plan and follow-up plan

Other

  • Patients with any missing baseline clinical and pathological information
  • The investigator believes that it is not suitable to participate in this clinical trial for any reason
  • Unable to provide informed consent

Who the study is looking for

  • Age ≥ 50 years
  • Patients must have histologically or cytologically confirmed prostate adenocarcinoma
  • PSA ≥ 20ng/ml or Gleason ≥ 8
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) score of 0-2
  • Life expectancy ≥ 6 months
  • Normal bone marrow function: absolute neutrophil count ≥ 1.5×109/L; platelets ≥ 75×109/L; hemoglobin ≥ 90g/L; white blood cell count ≥ 3.0×109/L
  • Normal liver function: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 2.5 times the upper limit of normal (ULN); for patients with liver metastasis, ALT/AST can be ≤ 5 times ULN
  • Total bilirubin ≤ 1.5 times ULN or total bilirubin \> 1.5 times ULN and direct bilirubin ≤ ULN;
  • Normal coagulation function: International Normalized Ratio(INR) ≤ 1.5, partial thromboplastin time (APTT) ≤ 1.5 times ULN, prothrombin time (PT) \< ULN + 4 seconds
  • Normal heart function: left ventricular ejection fraction (LVEF) ≥ 50%; corrected QT interval male \< 450ms, female \< 470ms, serum potassium ≥ 3.5mmol/L
  • Normal blood pressure: systolic blood pressure \< 140mmHg, diastolic blood pressure \< 90mmHg; patients with stable blood pressure assessment after appropriate clinical treatment can be enrolled
  • Normal renal function: serum creatinine ≤ 1.5 times ULN, and creatinine clearance ≥ 50 mL/min
  • Prospective subjects can understand and are willing to sign the informed consent form
  • Able to comply with the study visit schedule and other protocol requirements

Age in the registry: 50 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
Science and Technology Institute, Anhui Medical University
Coordinator of this site? Confirm its status
HefeiChinaRecruiting

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