Skip to content

Clinical study on evaluation of hematopoietic stem cell collection effect in patients with multiple myeloma based on lumbar multimodal MRI technology

Clinical study on evaluation of hematopoietic stem cell collection effect in patients with multiple myeloma based on lumbar multimodal MRI technology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084279
Enrollment
Unknown
Registered
2024-05-14
Start date
2024-06-20
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

multiple myeloma

Interventions

newly diagnosed multiple myeloma patients/ healthy donors:None

Sponsors

The second hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 18 years old = Age = 65 years old, regardless of gender VCD or VRD (which can be combined with daretouzumab) is used to induce the treatment of newly diagnosed multiple myeloma patients who intend to collect autologous hematopoietic stem cells for 3-4 courses or healthy donors who provide hematopoietic stem cells for allogeneic transplantation The score of ECOG physical state is =2 No serious complications, such as liver failure, renal failure, heart failure, etc. Non-pregnant and lactating women Be able to understand the test plan, follow the doctor's advice and sign the informed consent form.

Exclusion criteria

Exclusion criteria: Patients with relapsed and refractory multiple myeloma Have a history of arterial or venous thrombosis or thrombophilia in the past year Allergic to G-CSF or plerixafor Active infectious diseases, such as HBV, HCV and tuberculosis Serious diseases that may limit patients' participation in this trial (such as advanced infection, uncontrollable diabetes, severe cardiac insufficiency or myocardial infarction, hepatic and renal insufficiency, etc.) Those who are participating in other clinical trials or have participated in clinical trials of other drugs within 3 months Active malignant tumor Pregnant or lactating women Unable to understand or follow the research plan Any other circumstances that the researcher considers inappropriate to participate in this experiment.

Design outcomes

Primary

MeasureTime frame
CD34+ cell number;

Countries

China

Contacts

Public ContactJisong Yan

The second hospital of Dalian Medical University

yanjsdmu@126.com+86 177 0987 1028

Outcome results

None listed

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