Establishment of a Strategy for Preventing Graft-versus-host Disease After Allogeneic Hematopoietic Cell Transplantation by Exploring Immune Mechanisms of Regulatory and Effector T Cells
NCT ID: NCT07150468
Last Updated: 2025-09-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
146 participants
OBSERVATIONAL
2021-05-13
2025-08-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Interventions
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sampling blood
Sampling
1. patient
1. Peripheral blood samples in a volume of 25 cc will be collected before HCT and 2 weeks after HCT, and peripheral blood samples in a volume of 20 cc will be collected 4 weeks, 3 months, 6 months, and 12 months after HCT.
2. If GVHD occurs, additional blood sample (20 cc) will be collected.
3. In case of organ-specific GVHD including skin, gut, liver, muscle, etc., tissue samples from biopsy will be obtained for further analysis.
2. donor a. Peripheral blood samples in a volume of 20 cc will be collected before HCT
Eligibility Criteria
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Inclusion Criteria
2\. Family members: Family members of patients under 75 years of age who meet Criterion 1 and are willing to donate peripheral blood hematopoietic stem cells.
Exclusion Criteria
16 Years
75 Years
ALL
No
Sponsors
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Asan Medical Center
OTHER
Responsible Party
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Yunsuk Choi
Associate professor
Locations
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Asan Medical Center
Seoul, , South Korea
Countries
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Other Identifiers
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preventing GVHD after allo-HCT
Identifier Type: -
Identifier Source: org_study_id
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