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Multi-omics study of bladder cancer

Multi-omics study of bladder cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023992
Enrollment
Unknown
Registered
2019-06-21
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Bladder cancer

Interventions

Tumor group:Taking 4 ml of peripheral blood
non-tumor group:Taking 4 ml of peripheral blood

Sponsors

Shenzhen University Institute of Urology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.First-diagnosed and untreated bladder urothelial carcinoma. 2.Life expectancy is greater than 5 years and above. 3.Except for patients undergoing total cystectomy. 4.Willing to cooperate with sample collection and sustainable follow-up.

Exclusion criteria

Exclusion criteria: 1.Any of the following: immunodeficiency or damage (such as AIDS patients), immunosuppressive drugs or radiation therapy; fever and acute infectious diseases, including active tuberculosis, or receiving anti-tuberculosis treatment With severe chronic cardiovascular or cerebrovascular disease or chronic kidney disease; 2.Merging other organ tumors; 3.Those who have received chemotherapy, radiotherapy, or immunotherapy in the past 4 weeks (except for intravesical infusion chemotherapy immediately after surgery); 4.It is known or suspected that bladder perforation occurs during surgery; 5.Patients with severe urethral stricture can not be placed into the cystoscope; 6.Pelvic CT examination or full physical examination reports that the tumor has been metastasized; 7.Low immune function, congenital immunodeficiency disease, or history of organ transplantation; 8.Suffering from severe cardiovascular and cerebrovascular diseases such as myocardial infarction, severe or unstable angina pectoris, coronary/peripheral artery bypass surgery, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, or pulmonary embolism unable tolerate TURBT surgery; 9.There are obvious major visceral dysfunctions, such as: creatinine > 1.5 times the upper limit of the normal range, AST, ALT, total bilirubin > 1.5 times the upper limit of the normal range; 10.The body temperature of fever is over 38 °C, and there are obvious active infections that can affect clinical trials such as acute pneumonia, active tuberculosis, subjects with severe urinary tract infection, etc. 11.Patients rely on opioids or alcohol; 12.The investigator believes that there may be any situation that increases the risk of the subject or interferes with the execution of the clinical trial.

Design outcomes

Primary

MeasureTime frame
Blood test;Urinalysis;Transcriptome;Urine metabolome;Methylome;

Countries

China

Contacts

Public ContactSong Wu

Shenzhen University Institute of Urology

wusong@suz.edu.cn+86 18033411112

Outcome results

None listed

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