NCT00448357 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Experimental: GVHD prophylaxis Subjects with matched-related donors (MRDs) were treated with tacrolimus and methotrexate with or without alemtuzumab for graft vs host disease prophylaxis Subjects also receive busulfan and fludarabine . Matched unrelated donor (MUD) or mismatched related donor (MMRD) subjects receive GVHD prophylaxis with rabbit anti-thymocyte globulin (ATG) + Methotrexate Subjects also receive busulfan, fludarabine, and tacrolimus.
- id
- FG000
- title
- Experimental: GVHD Prophylaxis
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 54
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 54
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- A total of 55 subjects were consented, but one subject was not enrolled due to disease progression or death prior to protocol therapy.
- recruitment Details
- Patients with advanced, refractory, or high-risk hematologic cancers who were deemed suitable for myeloablative conditioning were recruited from one institution.
Complete source fields
- groups
- description
- Experimental: GVHD prophylaxis Subjects with matched-related donors (MRDs) were treated with tacrolimus and methotrexate with or without alemtuzumab for graft vs host disease prophylaxis Subjects also receive busulfan and fludarabine . Matched unrelated donor (MUD) or mismatched related donor (MMRD) subjects receive GVHD prophylaxis with rabbit anti-thymocyte globulin (ATG) + Methotrexate Subjects also receive busulfan, fludarabine, and tacrolimus.
- id
- FG000
- title
- Experimental: GVHD Prophylaxis
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 54
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 54
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- A total of 55 subjects were consented, but one subject was not enrolled due to disease progression or death prior to protocol therapy.
- recruitment Details
- Patients with advanced, refractory, or high-risk hematologic cancers who were deemed suitable for myeloablative conditioning were recruited from one institution.
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Preserved source evidence · Not medical advice
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