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CD9 in the progosis of amyloidosis

CD9 in the progosis of amyloidosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600128078
Enrollment
Unknown
Registered
2026-07-14
Start date
2025-10-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Amyloidosis(AL)

Interventions

Newly Diagnosed AL Amyloidosis Patient Group:None

Sponsors

The First Affiliated Hospital of Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18, = 3 months, and at least 1 year of follow-up can be completed.

Exclusion criteria

Exclusion criteria: 1. Merge other active malignant tumors (excluding basal cell carcinoma and cervical cancer in situ); 2. Previously received hematopoietic stem cell transplantation or CAR-T therapy; 3. Serious uncontrolled infections (active tuberculosis, HIV positive with CD4 <200/µ L, etc.); 4. NYHA grade IV or left ventricular ejection fraction <30%; 5. Pregnant or lactating women; 6. Unable to cooperate with follow-up due to mental illness or cognitive impairment; 7. Researchers have determined that bone marrow puncture is not suitable (due to severe coagulation disorders, anatomical abnormalities at the puncture site, etc.).

Design outcomes

Primary

MeasureTime frame
CD9;

Secondary

MeasureTime frame
NT-proBNP, Troponin, 24-hour urinary protein, creatinine clearance rate, bone marrow plasma cell ratio, lactate dehydrogenase, ß 2-microglobulin, albumin, hemoglobin, platelets;

Countries

China

Contacts

Public ContactQiang Zhuang

The First Affiliated Hospital of Wenzhou Medical University

zhuangqiang2007@163.com+86 577 55579482

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026