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The First Affiliated Hospital, Zhejiang University School of Medicine

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

This post hoc analysis included patients with acute leukemia who underwent allo-HSCT at the First Affiliated Hospital of Zhejiang University School of Medicine and Ruijin Hospital Shanghai Jiaotong University School of Medicine. Patients and their donors were assessed for eligibility to join this study. The inclusion criteria were: (1) age ≥ 5 years; (2) diagnosis of acute leukemia including acute myeloid leukemia, acute lymphocytic leukemia, and mixed phenotype acute leukemia; (3) patients attained complete remission (CR) and achieved full engraftment with 100% donor chimerism following allo-HSCT; (4) telomere testing was conducted on peripheral leukocytes of donors before granulocyte colony-stimulating factor (G-CSF) mobilization, and the results were obtained. Written informed consent was obtained from all included patients and their donors, and the study was conducted in compliance with the Declaration of Helsinki. Ethical approval was approved by the ethics review committee of the First Affiliated Hospital of Zhejiang University School of Medicine.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 5
Maximum Age: 90
Healthy Volunteers: t
View:

• Age ≥ 5 years

• First allo-HSCT from matched related, unrelated, or haploidentical donors

• Achievement of complete remission after allo-HSCT

• Donor blood sample collection before granulocyte colony-stimulating factor mobilization

Locations
Other Locations
China
Clinical research ethics committee of the first affiliated hospital, college of medicine, zhejiang University
RECRUITING
Hangzhou
Contact Information
Primary
He Huang, PhD&MD
huanghe@zju.edu.cn
+86 13605714822
Time Frame
Start Date: 2015-01-01
Estimated Completion Date: 2026-12-01
Participants
Target number of participants: 2500
Treatments
Donors aged 40 years or older
Donors aged < 40
Sponsors
Leads: Zhejiang University

This content was sourced from clinicaltrials.gov

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