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RECRUITINGOBSERVATIONAL

The Prospective Collection, Storage and Reporting of Data on Patients Undergoing Hematopoietic Stem Cell Transplantation Utilizing a Standard Preparative Regimen

The Prospective Collection, Storage and Reporting of Data on Patients

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

To provide the IRB approved mechanism for the prospective collection and analysis on participants who are undergoing either an autologous or allogeneic hematopoietic stem cell transplant for a disease in which a research question is not being addressed.

Who May Be Eligible (Plain English)

Who May Qualify: Planned standard of care dose intensive therapy and either an allogeneic or autologous bone marrow transplant Who Should NOT Join This Trial: Participation in any other treatment research protocol Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: Planned standard of care dose intensive therapy and either an allogeneic or autologous bone marrow transplant Exclusion Criteria: Participation in any other treatment research protocol

Locations (1)

Wake Forest Baptist Health
Winston-Salem, North Carolina, United States