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
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