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Early Screening for Prostate Cancer Based on Urinary Proteomics

Early Screening for Prostate Cancer Based on Urinary Proteomics

Status
Recruiting
Phases
Phase 3
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102395
Enrollment
Unknown
Registered
2025-05-14
Start date
2025-05-14
Completion date
Unknown
Last updated
2025-05-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

prostate cancer

Interventions

Patients with suspected prostate cancer undergoing prostate biopsy:none

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Inclusion Criteria for Prostate Cancer and Biopsy-Negative Patients1) Male, aged <= 85 years;2) Patients undergoing prostate biopsy for definitive diagnosis due to elevated PSA, positive digital rectal exam, or imaging indicative of suspected prostate cancer.Outpatients or inpatients who meet all of the above criteria and have collected pre-treatment urine samples can be included as subjects. Outpatients or inpatients who meet all of the above criteria and have collected urine samples can be included as subjects.

Exclusion criteria

Exclusion criteria: 1) Patients diagnosed with any malignant tumor within the past 5 years; 2) Patients who have previously undergone transurethral resection or ablation of the prostate; 3) Patients who have had prostate biopsies due to suspected prostate cancer; 4) Patients who have been on long-term anticoagulant or antiplatelet aggregation therapy (with anticoagulants stopped for less than 1 week); 5) Patients who have received any form of tumor treatment, including surgery, radiotherapy/chemotherapy, endocrine therapy, targeted therapy, and immunotherapy, within one month prior to blood draw for enrollment; 6) Patients with other severe systemic diseases that the investigator believes may interfere with the treatment, evaluation, and adherence of this trial, including severe respiratory, circulatory, neurological, psychiatric, digestive, endocrine, immune, and urinary system diseases; 7) Organ transplant recipients or those who have previously undergone non-autologous (allogeneic) bone marrow or stem cell transplants; 8) Subjects who had a blood transfusion within one month prior to blood draw; 9) Patients who are participating in other clinical trials, or who have participated in other clinical trials and completed them less than one year ago; 10) Patients whom the investigator deems unsuitable to participate in this clinical trial; any patient who meets any of the above criteria cannot be included as a subject.

Design outcomes

Primary

MeasureTime frame
ROC value;Specificity;

Countries

China

Contacts

Public ContactDi Gu

The First Affiliated Hospital of Guangzhou Medical University

sveong@163.com+86 188 1937 8495

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026