NCT00827099 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- 1. Fludarabine 30 mg\^m2 on days -7, -6, -5, -4 \& -3 2. Melphalan 140 mg\^m2 on day -2 3. Rabbit antithymocyte globulin (ATG) 6mg/kg divided over 3 days, Days -4,-3,-2. (Thymoglobulin 1.0mg/kg on day -4, and 2.5mg/kg/d on days -3, -2) 4. Tacrolimus starting on day -1 as a continuous infusion of 0.03 mg/kg/d. 5. Mycophenolate mofetil (MMF) IV 15mg/kg BID will start on Day 0
- id
- FG000
- title
- Umbilical Cord Blood Transplantation
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 5
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 5
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- There were no group assignments for this study. It was a single arm cord blood transplant study.
- recruitment Details
- Study was IRB approved on 6/8/06. The first patient was enrolled on 6/9/06. The last patient was enrolled on 12/22/08.
Complete source fields
- groups
- description
- 1. Fludarabine 30 mg\^m2 on days -7, -6, -5, -4 \& -3 2. Melphalan 140 mg\^m2 on day -2 3. Rabbit antithymocyte globulin (ATG) 6mg/kg divided over 3 days, Days -4,-3,-2. (Thymoglobulin 1.0mg/kg on day -4, and 2.5mg/kg/d on days -3, -2) 4. Tacrolimus starting on day -1 as a continuous infusion of 0.03 mg/kg/d. 5. Mycophenolate mofetil (MMF) IV 15mg/kg BID will start on Day 0
- id
- FG000
- title
- Umbilical Cord Blood Transplantation
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 5
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 5
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- There were no group assignments for this study. It was a single arm cord blood transplant study.
- recruitment Details
- Study was IRB approved on 6/8/06. The first patient was enrolled on 6/9/06. The last patient was enrolled on 12/22/08.
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Preserved source evidence · Not medical advice
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