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Analysis of immune reconstitution after haploid allogenic hematopoietic stem cell transplantation at single-cell level

Analysis of immune reconstitution after haploid allogenic hematopoietic stem cell transplantation at single-cell level

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400082585
Enrollment
Unknown
Registered
2024-04-01
Start date
2024-04-01
Completion date
Unknown
Last updated
2024-04-08

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

Conditions

Acute myelogenous leukemia

Interventions

Post-transplantation group of AML patients:NA

Sponsors

Medical Center of Hematology, the Second Affiliated Hospital of the Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: ? Acute Myeloid Leukemia (AML) diagnosed from March 2024 to March 2026 (intermediate-risk assessment according to NCCN), donors of both sexes, aged 18-50 years, with indications for transplantation and eligible for haploidentical hematopoietic stem cell transplantation. ?KPS score >60 points, predicted survival time >6 months; ? without serious damage of vital organs: ? creatinine 55%; ? heme >9g/dL, bilirubin 0.5×109/L, platelet >20×109/L); ? Stable control of primary blood diseases, no other contraindications of hematopoietic stem cell transplantation; ? Voluntarily participated in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: ? There is active bleeding caused by drugs or thrombocytopenia; ? Pregnant or lactating women; ? Severe heart, kidney or liver dysfunction; ? combined with other malignant tumors requiring treatment; ? Inability to understand or follow the study protocol due to clinical symptoms of brain dysfunction or severe mental disease; ? patients who are unable to complete the necessary treatment plan and follow-up observation; ? patients with severe acute allergic reaction; ? clinical uncontrolled active infection; ? Investigators felt that other reasons were not appropriate for clinical trialists.

Design outcomes

Primary

MeasureTime frame
10×Genomics Single Cell Transcriptome Sequencing;Co-profiling; Smart-seq3, based on Switching mechanism at the 5’end of the RNA template technology;

Countries

China

Contacts

Public ContactXi Zhang

The Second Affiliated Hospital of the Army Medical University

zhangxxi@sina.com+86 138 0831 0064

Outcome results

None listed

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