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The Prospective Collection, Storage and Reporting of Data on Patients Undergoing Hematopoietic Stem Cell Transplantation Utilizing a Standard Preparative Regimen
RECRUITINGSponsored by Wake Forest University Health Sciences
Actively Recruiting
SponsorWake Forest University Health Sciences
Started2001-05-21
Est. completion2026-06
Eligibility
Age18 Years – 120 Years
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT01890486
Summary
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.
Eligibility
Age: 18 Years – 120 YearsHealthy volunteers accepted
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
Conditions11
Acute Lymphocytic LeukemiaAcute Myelogenous LeukemiaCancerChronic Lymphocytic LeukemiaChronic Myelogenous LeukemiaGerm Cell NeoplasmsHodgkin's DiseaseImmunodeficiency DiseasesMultiple MyelomaMyelodysplastic Syndromes
Locations1 site
Wake Forest Baptist Health
Winston-Salem, North Carolina, 27157
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
SponsorWake Forest University Health Sciences
Started2001-05-21
Est. completion2026-06
Eligibility
Age18 Years – 120 Years
Healthy vol.Accepted
Locations1 site
View on ClinicalTrials.gov →
NCT01890486