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Clinical Trial Summary

This trial plans to enroll 190 eligible patients and randomize them into two groups with a 1:1 ratio, with 95 patients in each group. The experimental group will receive immediate cryoablation therapy at the resection site after TUR, while the control group will only undergo TUR and receive conventional BCG instillation therapy postoperatively. Both groups of subjects will undergo Re-TURBT or cystoscopy 10-12 weeks after surgery to compare the tumor-free residual rates and adverse events between the two groups.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06324058
Study type Interventional
Source Huashan Hospital
Contact Shenghua Liu, Dr.
Phone +8618101881202
Email 08301010098@fudan.edu.cn
Status Not yet recruiting
Phase N/A
Start date March 18, 2024
Completion date March 18, 2026

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