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A single-center, randomized controlled study on the treatment of bone marrow suppression after autologous hematopoietic stem cell transplantation with G-CSF combined with leucogen

A single-center, randomized controlled study on the treatment of bone marrow suppression after autologous hematopoietic stem cell transplantation with G-CSF combined with leucogen

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103184
Enrollment
Unknown
Registered
2025-05-26
Start date
2025-05-30
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Myelosuppression after autologous hematopoietic stem cell transplantation

Interventions

intervention group:G-CSF combined with leucogen
Control group:G-CSF

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-70 years old, gender unlimited; 2.Autologous hematopoietic stem cell transplantation for patients with blood diseases; 3.Overall Physical Status Score (ECOG) 0-2; 4.Estimated survival time > 3 months; 5.Study participants volunteered to participate in the study, had a good understanding of the treatment and follow-up received in the study program, were able to understand the study process, and voluntarily signed informed consent;

Exclusion criteria

Exclusion criteria: 1.There are other major complications of heart, liver and kidney; 2.Patients with myelodysplastic symptoms; 3.Hyperelevated blood cell drugs were used within 2 weeks before enrollment; 4.During the pretreatment period, radiotherapy was accompanied by chemotherapy; 5.Patients allergic to G-CSF or leucogen; 6.Hiv-positive patients; 7.Patients with poor compliance or mental abnormalities; 8.Patients with potentially life-threatening or severe organ dysfunction were deemed unfit to participate in the study;

Design outcomes

Primary

MeasureTime frame
Neutrophil engraftment time;

Secondary

MeasureTime frame
Platelet engraftment time;Febrile Neutropenia (FN) incidence rate;total platelet transfusion volume;

Countries

China

Contacts

Public ContactDongfeng Zeng

Army Medical Center of PLA

dongfengzeng@hotmail.com+86 23 68746231

Outcome results

None listed

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