About this trial
Background Urothelial carcinoma (UC) is the most common malignancy of the urinary system. Hematuria is a significant clinical manifestation of UC, often diagnosed through invasive procedures. Urine DNA methylation testing is a promising non-invasive method for early UC detection.
Objectives To evaluate the sensitivity and specificity of urine DNA methylation testing for detecting UC in patients with hematuria, using standard clinical and pathological diagnoses as the gold standard. This study also aim to investigate the association between preoperative urine DNA methylation status and prognosis in UC patients.
For non-UC patients: Follow up for one year to assess the risk of UC development based on preoperative urine DNA methylation status.
Sample Size Calculation Expected sensitivity: 86% Expected specificity: 90% Significance level (Alpha): 0.05 Total participants needed: 1053 (adjusted for 5% dropout rate, 1109 participants will be recruited).
Study Procedure Enrollment and Sample Collection: Screen patients, obtain consent, collect urine samples.
Blinding and Testing: Blinded sample processing and DNA methylation testing. Unblinding and Analysis: Statistical analysis of sensitivity and specificity. Reporting: Compilation and consolidation of clinical trial reports.
Urine DNA methylation testing is expected to demonstrate high sensitivity and specificity for diagnosing urothelial carcinoma (UC) in patients with hematuria. This non-invasive diagnostic method promises to deliver valuable information, potentially leading to improved patient outcomes.
Eligibility criteria
Qualifiers
Aged between 18 and 99 years, with gross or microscopic hematuria (RBC ≥ 3 /HPF or RBC > 18 /μL for men, > 33 /μL for women).
Able to provide 50ml urine for testing before surgery.
Consent to participate in the study and sign the informed consent form.
Disqualifiers
With history of any malignancies (including UC).
Severe urinary tract infection leading to sepsis.
Patients with indwelling catheters, nephrostomy, or cystostomy.
Severe liver or kidney failure or other conditions deemed unsuitable for the study.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Changhai Hospital
Lead sponsor
RenJi Hospital
Collaborator
First Hospital of China Medical University
Collaborator
Tongji Hospital
Collaborator