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Recruiting Observational

Establishment and Promotion of an AI-Based Early Warning System for Prostate and Bladder Cancer Screening in the Male Community Population of Beijing

NCT07319923 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2024-01-01
Last updated
2026-01-06

Condition(s) studied

Prostate CancerCommunity-based Screening

Investigational drug(s) / intervention(s)

No intervention

No intervention: No intervention

Study summary

Prostate cancer is one of the most common malignancies in the male genitourinary system, and it is also the cancer with the fastest-growing incidence and mortality rates among men in China. Although prostate cancer screening can significantly reduce mortality, China has not yet established a well-developed screening system, which is one of the reasons why its mortality rate remains notably higher than that of Western countries. The primary objective of this project is to establish an efficient screening-diagnosis-treatment pathway, beginning with screening in community hospitals, followed by definitive diagnosis in secondary hospitals, and finally treatment in tertiary hospitals. Additionally, the project aims to achieve multi-institutional and multi-terminal sharing of disease information as well as dynamic monitoring and follow-up. The feasibility and effectiveness of this model will be validated through statistical analysis of the data.

Eligibility

Sex
ALL
Min age
18 Years
Max age
85 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Male community residents aged 50 years or older; Life expectancy \> 10 years and ECOG performance status of 0-2; Permanent residents of Beijing who are willing to cooperate with researchers in the screening process, complete required tests and questionnaires, and participate in subsequent follow-up; Support for the research project and provision of signed informed consent. Exclusion Criteria: * 1)Presence of any other malignant tumor or pre-existing prostate malignancy; 2)Presence of prostatitis or active infection in other parts of the urinary system; 3)Inability to cooperate with the study procedures or other factors deemed unsuitable for participation in this study.

Primary outcome measure(s)

  • Serum PSA level — from 2025 to 2027

Trial sites (1)

FacilityCityRegionStatus
Department of Urology, Peking University First Hospital, Beijing, 100034 Beijing China Recruiting
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 NCT07319923 on ClinicalTrials.gov ↗ ← All trials in China