Skip to content

Clinical research on the detection of lymphoma pathological characteristics using flow cytometry

Clinical research on the detection of lymphoma pathological characteristics using flow cytometry

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082064
Enrollment
Unknown
Registered
2024-03-20
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Lymphoma

Interventions

Gold Standard:Interpret as gold standard based on immunohistochemistry test results. Immunohistochemical method: Biomarkers include CD3/CD20/CD4/CD8/TIM3/LAG3
The equipment includes an immunohistochemical staining machine.
Index test:Flow cytometry method: Biomarkers include CD3/CD20/CD4/CD8/TIM3/LAG3
The equipment includes a flow cytometer

Sponsors

Sichuan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as lymphoma by histopathology; 2. Do not distinguish between age, gender, lymph nodes inside and outside 3. The expected survival time is more than 6 months; 4. No uncontrolled activity infection lesions; 5. Be able to understand this test, and sign the "Informed consent form"; Sample size: at least 0.5cm3; samples within 24 hours from the body, save in culture medium at 2-8 ?; not soak in fixed liquids such as formalin.

Exclusion criteria

Exclusion criteria: 1. Severe heart dysfunction, left ventricular ejection score <50 2. Have a history of severe pulmonary dysfunction disease 3. Merge other malignant tumors 4. Combined severe infection and cannot be effectively controlled 5. Consolidated serious autoimmune or congenital immune defects 6. Researchers believe that it may increase the results of the subject's danger or interference test results Sample size: less than 0.5cm3; more than 24 hours from the body and no refrigeration; sample soaking in fixed liquid.

Design outcomes

Primary

MeasureTime frame
CD3/CD20/CD4/CD8/TIM3/LAG3;CD3/CD20/CD4/CD8/TIM3/LAG3;Accuracy;Sensitivity;

Secondary

MeasureTime frame
Specifity;

Countries

China

Contacts

Public ContactYang Liu

Sichuan Cancer Hospital

liuyang@scszlyy.org.cn+86 189 0091 0317

Outcome results

None listed

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