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Establishment of a New Precise Diagnosis and Treatment System for Urothelial Carcinoma Based on Artificial Intelligence and Multimodal Multi-Omics Mass Spectrometry Platform

Establishment of a New Precise Diagnosis and Treatment System for Urothelial Carcinoma Based on Artificial Intelligence and Multimodal Multi-Omics Mass Spectrometry Platform

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500102174
Enrollment
Unknown
Registered
2025-05-09
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-12

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

Conditions

Urothelial carcinoma

Interventions

Index test:A multi-omics early model based on patient urine mass spectrometry results, serum mass spectrometry results, imaging data, and clinical information

Sponsors

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 18 years. 2. Patients diagnosed with urothelial carcinoma or benign urological diseases (including but not limited to urinary calculi, benign prostatic hyperplasia, and benign urological tumors) at multiple centers with Sir Run Run Shaw Hospital as the the leading center, or healthy individuals undergoing routine physical examinations. 3. Voluntary participation in this study with signed informed consent. If a participant is unable to read or sign the informed consent form due to incapacity (e.g., lack of legal competence), their legal guardian must complete the informed consent process and sign on their behalf. If a participant is unable to read the informed consent form (e.g., illiterate participants), the informed consent process must be witnessed by an impartial witness, who will also sign the consent form.

Exclusion criteria

Exclusion criteria: 1. Individuals currently menstruating. 2. Vulnerable populations, excluding critically ill patients/elderly individuals/illiterate individuals/ people with mental illnesses/ people with cognitive impairments/ pregnant women, etc.

Design outcomes

Primary

MeasureTime frame
Specificity;Sensitivity;

Countries

China

Contacts

Public ContactGuoqing Ding

Sir Run Run Shaw Hospital, Zhejiang University School of Medicine

3196014@zju.edu.cn+86 138 6743 8309

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026