AI-Guided TURBT for Bladder Cancer
Starting soon · Not applicable
Conditions studied: Bladder Cancer
In brief
This prospective, randomized, controlled, single-center study evaluates whether an AI navigation planning system used during Transurethral Resection of Bladder Tumor (TURBT) can improve recurrence-free survival in patients with non-muscle invasive bladder cancer. Participants are randomized to receive either standard TURBT surgery or standard TURBT with AI-assisted real-time tumor identification and resection margin guidance. The primary outcome is recurrence-free survival, with secondary outcomes including surgical duration, intraoperative blood loss, perioperative bleeding, and complication rates. The study aims to provide high-level evidence on the clinical utility of AI-assisted surgical navigation in bladder cancer treatment.
Key facts
- Study ID
- NCT07727343
- Run by
- Fudan University
- People needed
- 170
- Starts
- 2026-08-01
- Expected to finish
- 2028-11-30
- Last updated by the study team
- 2026-07-27
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age between 18 and 75 years, male or female.
- Clinical or imaging diagnosis of non-muscle invasive bladder cancer (NMIBC) according to international diagnostic standards (CT, MRI, ultrasound, cystoscopy).
- Medically fit for TURBT surgery, with normal or essentially normal renal, cardiopulmonary, and hepatic function.
- Willing and able to provide written informed consent (signed by the patient or a legally authorized representative).
You may not qualify if…
- Pregnant or lactating women.
- Severe dysfunction of other vital organs (heart, lungs, kidneys, etc.).
- Imaging evidence of distant metastases.
- Severe infection or active inflammation.
- Psychiatric disorders or inability to comply with study procedures.
- Any other condition deemed by the investigator as inappropriate for participation.
Full record on ClinicalTrials.gov
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