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Study identifier: NCT07036731 Synced from ClinicalTrials.gov · July 28, 2026
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A Study Comparing the Necessity of a Second Transurethral Resection in High-Risk Non-Muscle-Invasive Bladder Cancer Patients With Negative Results From Post-Initial Resection Urine Genome-Wide Low-Depth Sequencing

Condition: Non Muscle Invasive Bladder Cancer  ·  Sponsor: The First Affiliated Hospital with Nanjing Medical University

PhaseNA
Planned participants428
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

This study is a prospective, randomized, multicenter clinical trial aiming to enroll 428 patients with non-muscle-invasive bladder cancer (NMIBC) from the Department of Urology at Jiangsu Provincial People's Hospital and its affiliated centers, who have undergone their initial transurethral resection and are scheduled for a second resection. Within 1-6 weeks after the first resection and prior to the second resection, 100ml of routine urine will be collected and sent within 24 hours to Beijing Genetron Health Clinical Laboratory Co., Ltd. for the extraction of urinary sediment DNA, which will then undergo genome-wide low-depth sequencing. Patients with positive test results will proceed with the second resection, while those with negative results will be randomly assigned in a 1:2 ratio to either the intervention group, which will not undergo a second resection, or the control group, which will undergo the second resection. All enrolled patients will be followed up for two years. The study will statistically analyze and compare the two-year recurrence-free survival rates between the two groups and evaluate the predictive capability of the test results for follow-up recurrence.

This description comes directly from the study's public registry record.

Talk to the study team

Yang xiao, PhD  ·  +8613951813528  ·  yangxiao2915@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029Nanjing, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07036731