NCT00998049 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Plerixafor 160mg/kg/dose by IV on days 5-8 Filgrastim (G-CSF) 10 mg/kg/dose subcutaneously on days 1-8.
- id
- FG000
- title
- Plerixafor
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- One participant was deemed ineligible and is excluded from all analyses per study design.
- recruitment Details
- Forty (40) participants were recruited at Mayo Clinic (Rochester, Florida and Arizona) between December 2009 and October 2011.
Complete source fields
- groups
- description
- Plerixafor 160mg/kg/dose by IV on days 5-8 Filgrastim (G-CSF) 10 mg/kg/dose subcutaneously on days 1-8.
- id
- FG000
- title
- Plerixafor
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- One participant was deemed ineligible and is excluded from all analyses per study design.
- recruitment Details
- Forty (40) participants were recruited at Mayo Clinic (Rochester, Florida and Arizona) between December 2009 and October 2011.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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