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Center for International Blood and Marrow Transplant Research

Protocols & Consent Forms

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CIBMTR encourages centers to invite transplant recipients and donors to participate in CIBMTR's Research Database and the CIBMTR Biorepository.

To participate in the Research Database and the CIBMTR Biorepository studies, centers must have IRB approval of the study’s protocol and informed consent document(s). See each study’s page below for additional information. The PRO Data Collection study is managed centrally by CIBMTR and does not need to be submitted to center IRBs.

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Research Database Protocol

This database includes recipient baseline and outcome data for related and unrelated allogeneic transplants from any cell source, autologous transplants, and other cellular therapies including CART and gene therapies. Data are also collected on unrelated donors.

CIBMTR Biorepository

The CIBMTR Biorepository contains cell and serum samples collected from related and unrelated transplant donors, cord blood units, and recipients.

PRO Data Collection Protocol

CIBMTR collects longitudinal or cross-sectional PRO data from recipients of cellular therapies who are also enrolled in the Protocol for a Research Database for Hematopoietic Cell Transplantation, Other Cellular Therapies, and Marrow Toxic Injuries (Research Database protocol).