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A prospective cohort study on establishing a precision diagnosis and treatment system for bladder cancer based on multi-omics

A prospective cohort study on establishing a precision diagnosis and treatment system for bladder cancer based on multi-omics

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125303
Enrollment
Unknown
Registered
2026-05-25
Start date
2025-09-19
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Bladder cancer

Interventions

Observation group:None

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients must be 18 years or older and under 90 years old at the time of signing the informed consent form; 2. Patients must have pathologically confirmed urothelial bladder cancer; 3. Expected survival >12 months; 4. Eastern Cooperative Oncology Group performance status 0-2; 5. Patients must agree and be able to attend scheduled study visits, provide blood, urine, and surgical specimens during the specified treatment period, provide clinical information, and cooperate with other study procedures; 6. Patients must have normal organ function, a white blood cell count >= 3000/mm^3 or an absolute neutrophil count =1500/mm^3, and aspartate aminotransferase (AST. and alanine aminotransferase (ALT. <=1.5 ULN.

Exclusion criteria

Exclusion criteria: 1. Patients who, in the investigator's judgment, have other serious illnesses that may affect follow-up and short-term survival, or who have any medical condition indicating a significant risk of death during the 1-year study period. 2. Patients who have had any other malignant tumor within 3 years prior to enrollment. 3. Patients whose clinical information required for the study is unavailable. 4. Patients who, in the investigator's opinion, are otherwise unsuitable for enrollment.

Design outcomes

Primary

MeasureTime frame
RNA sequencing;Single-cell sequencing;Progression-Free Survival (PFS);

Secondary

MeasureTime frame
Overall Survival (OS);

Countries

China

Contacts

Public ContactMinfeng Chen

Xiangya Hospital, Central South University

chenminfeng1999@csu.edu.cn+86 135 1731 9380

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026