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UROCAD-Guided Noninvasive Surveillance versus Standard Cystoscopic Surveillance for Intermediate- and High-Risk Non-Muscle-Invasive Bladder Cancer: A Multicenter Randomized Controlled Trial

A Multicenter Randomized Controlled Trial Comparing UROCAD-Based Noninvasive Surveillance with Standard Cystoscopic Surveillance for Intermediate- and High-Risk Non-Muscle-Invasive Bladder Cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127901
Enrollment
Unknown
Registered
2026-07-09
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

intermediate/high-risk non-muscle-invasive bladder cancer

Interventions

control group:Standard cystoscopy follow-up every 3 months for 2 years
intervention group:UROCAD-guided follow-up

Sponsors

Zhejiang Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. Pathologically confirmed intermediate- or high-risk NMIBC (including T1, CIS, high-grade Ta, multiple, or recurrent tumors); 3. Completed TURBT and immediate intravesical instillation therapy; 4. No imaging evidence indicating upper urinary tract tumors or distant metastasis within 3 months postoperatively; 5. ECOG performance status of 0-2; 6. Expected to complete the 24-month follow-up; 7. Voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Previous or concurrent presence of muscle-invasive bladder cancer, upper tract urothelial carcinoma, or other malignant tumors; 2. Presence of macroscopic residual tumor after surgery; 3. Severe cardiac, hepatic, or renal dysfunction; 4. Immunodeficiency or long-term use of immunosuppressants; 5. Pregnant or lactating women; 6. Recent participation in other clinical trials; 7. Other conditions considered unsuitable for participation by the investigator.

Design outcomes

Primary

MeasureTime frame
2-year high-grade recurrence-free survival;

Secondary

MeasureTime frame
2 years of progression-free survival;2-year recurrence-free survival;Number of cystoscopy examinations;

Countries

China

Contacts

Public ContactChuanliang Xu

Zhejiang Cancer Hospital

chuanliang_xu@126.com+86 21 3116 1716

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026