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Clinical Trial Summary

This study prospectively included 178 patients with bladder neoplastic lesions who planned to undergo surgery (with or without preoperative neoadjuvant chemotherapy). Inclusion criteria: Patients with pathologically confirmed bladder cancer after radical or partial cystectomy or TURBT (< 2 weeks between surgical resection and imaging). Exclusion criteria: 1) Prior history of chemotherapy and/or radiotherapy; 2) No surgical resection; 3) The interval between surgical resection and imaging examination is > 2 weeks; 4) Obvious artifacts; 5)MRI scan contraindications. All subjects underwent pelvic MRI. Data was collected using a Siemens VIDA 3TMR scanner (Siemens Healthcare, Erlangen, Germany). All subjects underwent standardized scanning protocols. The obtained images are post-processed and the experimental results are analyzed statistically.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06033040
Study type Observational [Patient Registry]
Source Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Contact Yuan Luo, master
Phone 8618816791193
Email luoy289@mail2.sysu.edu.cn
Status Recruiting
Phase
Start date August 15, 2023
Completion date December 31, 2025

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