Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06912672

Performance Evaluation of a Urine-based Methylation Assay for Urothelial Carcinoma

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. To evaluate the sensitivity and specificity of urine DNA methylation testing for detecting UC, using standard clinical and pathological diagnoses as the gold standard.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

About this study

Urothelial carcinoma (UC) is the most common malignancy of the urinary system, and early detection and diagnosis are crucial for patient prognosis. Hematuria is a significant clinical manifestation of UC, but its diagnosis often relies on invasive procedures and imaging, posing a substantial burden on patients. With the advancement of molecular biology techniques, urine DNA methylation testing has emerged as a non-invasive and highly sensitive method for early UC detection. This study aims to evaluate the performance of urine DNA methylation testing in detecting UC in patients with hematuria.

All patients with hematuria will receive standard clinical diagnosis, including examinations, tests, surgeries, and pathological assessments to determine the presence of UC. These clinical diagnoses will serve as the gold standard to evaluate the sensitivity and specificity of urine DNA methylation testing in detecting UC in patients with hematuria.

To ensure accuracy and reliability of the results, select a subset of samples with known test results for external methylation sequencing. Authorized researchers will unblind the samples, and the statistical team will analyze the results, calculating sensitivity, specificity, positive predictive value, and negative predictive value of the urine DNA methylation test.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged between 18 and 90 years, with gross or microscopic hematuria.
  • Able to provide enough urine for testing before surgery.
  • Consent to participate in the study and sign the informed consent form.

Exclusion criteria

  • With history of any malignancies (including Urothelial carcinoma).
  • 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.
  • Samples with insufficient DNA content or other quality control failures.
  • Incomplete clinical or pathological data.
  • Patients currently undergoing intravesical or systemic chemotherapy, radiotherapy, immunotherapy, or targeted therapy.

Treatment and study plan

Evaluate the diagnostic performance of EPIPROBE TAGMe DNA Methylation Detection Kit for Urothelial Cancer

Diagnostic Test

The study aims to evaluate the diagnostic performance of the EPIPROBE TAGMe DNA Methylation Detection Kit for the detection of urothelial cancer. This assay utilizes targeted DNA methylation analysis to identify specific epigenetic alterations associated with urothelial malignancies. The performance of the kit will be assessed in terms of sensitivity, specificity, and overall diagnostic accuracy using clinical urine samples from a patient population with hematuria.

Primary outcomes

  1. Diagnostic performance of DNA methylation test for urothelial carcinoma

    Time frame: 2 weeks

    Evaluate the diagnostic performance of EPIPROBE TAGMe DNA Methylation Detection Kit for Urothelial Cancer by calculating the sensitivity, specificity.

Study contacts

Contact information is provided by the study sponsor or research team.

Yaping Dong

CONTACT

[email protected]

86-18046043049

Sponsors and collaborators

Lead sponsor

Shanghai Epiprobe Biotechnology Co., Ltd.

Industry

Collaborators

  • Changhai Hospital
  • First Hospital of China Medical University
  • RenJi Hospital
  • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
  • Tongji Hospital

Registry information

Official study title

Performance Evaluation of a Urine-based Methylation Assay for Urothelial Carcinoma in Patients With Hematuria: A Prospective, Multi-center Cohort Study

Acronym: UMT-UC

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Apr 6, 2025
Registry last updated
Apr 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.