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A Prospective Study Evaluating the Efficacy and Safety of Romiplostim in Platelet Recovery Following Allogeneic Hematopoietic Stem Cell Transplantation

A Prospective Study Evaluating the Efficacy and Safety of Romiplostim in Platelet Recovery Following Allogeneic Hematopoietic Stem Cell Transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120742
Enrollment
Unknown
Registered
2026-03-19
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Platelet Reconstitution after Allogeneic hematopoietic stem cell transplantation

Interventions

Romiplostim intervention group:Starting 4 days after transplantation, administer Romosozumab 250 µg per dose subcutaneously, once a week, until 60 days after transplantation.

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Participants provided voluntary, written informed consent prior to enrollment and demonstrated consistent adherence to the study protocol, including full cooperation with all scheduled follow-up assessments. 2.Participants met established clinical indications for allogeneic hematopoietic stem cell transplantation (allo-HSCT), fulfilled pre-transplant eligibility criteria based on comprehensive physical examination and laboratory evaluation, and were scheduled to undergo allo-HSCT at the First Affiliated Hospital of Xi’an Jiaotong University. 3.Pre-transplant peripheral blood platelet count was =50 × 10?/L, and bone marrow examination confirmed a normal megakaryocyte count. 4. Age between 18 and 70 (inclusive);

Exclusion criteria

Exclusion criteria: 1.Patients diagnosed with primary or secondary myelofibrosis, as well as those with acute leukemia transformed from myelofibrosis. 2.Patients with antiphospholipid syndrome or hereditary thrombophilia before transplantation, and those whose researchers judge that the risk of thrombosis after transplantation is high; 3.Other situations where researchers determine that the patients are not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Platelet reconstitution time;

Countries

China

Contacts

Public ContactRen Juan

The First Affiliated Hospital of Xi'an Jiaotong University

timeflyrj@126.com+86 29 8532 3514

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026