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Application of Urine Nucleic Acid in Non-invasive Diagnosis of Bladder Cancer

Application of Urine Nucleic Acid in Non-invasive Diagnosis of Bladder Cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000029980
Enrollment
Unknown
Registered
2020-02-18
Start date
2020-02-20
Completion date
Unknown
Last updated
2020-02-25

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

Conditions

bladder cancer

Interventions

Gold Standard:Cystoscope and related pathological diagnosis
Index test:Urinary DNA

Sponsors

Department of Urology, Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Suspected bladder cancer patient with signs and symptoms of urinary tract inflammation (painless gross hematuria, urine routine occult blood, frequency of urination, urgency of urination, pain in urination, etc.), age > 18 years old. 2. The clinical samples of each clinical trial object should be fresh and sufficient for examination reagent and routine urine test. 3. All samples are from outpatient or inpatient specimens of clinical hospitals, and all samples must have clinical diagnosis or pathological diagnosis. 4.All samples should have corresponding basic clinical information, including sample ID number (outpatient number, medical record number, contact information and hospital number), gender, age, smoking history, chemical exposure history, family history of bladder cancer and clinical diagnosis information. 5. Control cases of other urinary tract diseases other than bladder cancer (which were eventually clinically diagnosed as non-bladder cancer), including prostatic hyperplasia, urinary tract stones, urinary tract infection, kidney cancer, etc.

Exclusion criteria

Exclusion criteria: 1. Sample number (outpatient number, medical record number or hospital number, etc.), gender, age, clinical diagnosis and other information missing. 2. Samples are not fresh. 3. The sample size is not enough to complete all the test samples. 4. Other samples that do not meet the basic requirements of examination reagent or comparison method.

Design outcomes

Primary

MeasureTime frame
Urinary DNA;Urinalysis;SPE, SEN, ACC;methylation;

Countries

China

Contacts

Public ContactLong Wang

Department of Urology, Xiangya Hospital, Central South University

doctorwanglong@163.com+86 13873151645

Outcome results

None listed

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