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Clinical Trial Summary

The primary objective of this clinical trial is to determine the sensitivity and specificity of the EarlyTect® Bladder Cancer test for bladder cancer among patients with hematuria by comparing it to the results of cystoscopy examinations. The second objective is to compare the clinical performance of EarlyTect® Bladder Cancer test with a NMP22 test and urine cytology test with respect to bladder cancer. By histopathological examination, lesions identified during cystoscopy will be confirmed as malignant or non-malignant by histological examination.


Clinical Trial Description

Patients with hematuria who are scheduled for cystoscopy will be asked to collect a urine sample for EarlyTect® Bladder Cancer test and will undergo NMP22 and urine cytology tests. The participants will undergo a cystoscopy within 30 days of enrollment. For confirmation of the diagnosis and stage of the tumor, representative histopathology slides from TURBT (Transurethral Resection of Bladder Tumors) may be retrieved and examined by the central pathology laboratory. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05220189
Study type Observational
Source Asan Medical Center
Contact Cheol Kwak, MD PhD
Phone 82-2-2072-0817
Email mdrafael@snu.ac.kr
Status Recruiting
Phase
Start date February 3, 2022
Completion date January 31, 2024

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