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An efficient method of eliminating M protein in patients with multiple myeloma by Plasma-free replacement

An efficient method of eliminating M protein in patients with multiple myeloma by Plasma-free replacement

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000030640
Enrollment
Unknown
Registered
2020-03-08
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-09-07

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

Conditions

Multiple myeloma

Interventions

Not grouped:Plasma-free replacement

Sponsors

Department of Hematology, Zhongnan Hospital, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with MM confirmed by bone marrow morphology and immunology; 2. Patients with a stable condition after routine treatment; 3.Patients with renal insufficiency or M protein abnormalities; 4.60-80 years old; 5.With liver and kidney function: blood bilirubin <= 35µmol / L, AST / ALT below 2 times the upper limit of normal value, blood creatinine <= 150µmol / L; 6. With normal heart function; 7. Physical condition score 0-2 (ECOG score); 8. Get informed consent from patient or family member.

Exclusion criteria

Exclusion criteria: 1. Patients with allergies or obvious contraindications to any drug involved in the program; 2. With severe heart disease, including myocardial infarction and cardiac insufficiency; 3.With malignant tumors of other organs; 4.With active phase of TB patients and HIV positive patients; 5.Patients with other blood system diseases at the same time; 6. Pregnant or lactating women; 7. Patients who do not understand or follow the protocol; 8. With previous history of intolerance or allergy to similar drugs; 9. Patients who are also participating in other clinical researchers; 10. Any other circumstances that hinder the study.

Design outcomes

Primary

MeasureTime frame
M protein content in plasma;

Secondary

MeasureTime frame
Blood routine;Liver and kidney function;Patient complication rate;Assess patient symptoms;Neutrophil recovery time;Hemoglobin recovery time;Platelet recovery time;

Countries

China

Contacts

Public ContactFuling Zhou

Department of Hematology, Zhongnan Hospital, Wuhan University

zhoufuling@whu.edu.cn+86 18986265580

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026