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Diagnostic test for urothelial carcinoma using cellular glycose metabolism (immunofluorescent techniques)

Diagnostic test for urothelial carcinoma using cellular glycose metabolism (immunofluorescent techniques)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200058024
Enrollment
Unknown
Registered
2022-03-27
Start date
2022-04-01
Completion date
Unknown
Last updated
2023-11-27

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

Conditions

urothelial carcinoma

Interventions

Gold Standard:Urine cytology
Index test:Diagnostic kit of cellular glucose metabolism (immunofluorescence techniques)

Sponsors

Junhealth Biotechnology Co. Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Group A (suspected bladder cancer patients) : (1) Meet one of the following conditions: 1) Imaging suggests space occupying in the bladder cavity; 2) Gross hematuria; 3) A history of uroepithelial cancer with high-risk recurrence factors (>=T1, G3, multiple, recurrence frequency >=1 / year); (2) Aged >=18 years, gender unlimited; (3) The patient is willing to provide a urine sample for testing; (4) The patient can provide adequate urine samples that meet the requirements of various detection methods. 2. Group B (non-bladder cancer patients) : (1) Aged >=18 years, gender unlimited; (2) The patient is willing to provide a urine sample for testing; (3) The patient can provide adequate urine samples that meet the requirements of various detection methods.

Exclusion criteria

Exclusion criteria: 1. Had undergone transurethral invasive operation within 1 month before enrollment; 2. Received therapeutic infusion chemotherapy, BCG vaccine, systemic chemotherapy, immunotherapy, etc., within 3 months before enrollment; 3. The patient had a history of other malignant tumors; 4. Poor patient compliance, unable to complete regular follow-up; 5. Sample collection and processing of samples that do not meet the requirements of standard laboratory operations and product specifications; 6. Other conditions for which the investigator judged the patient unsuitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Sensitivity;

Countries

China

Contacts

Public ContactJiang Haowen

Huashan Hospital Fudan University

urology_hs@163.com+86 18121186785

Outcome results

None listed

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