NCT01208103 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Capecitabine 750 mg/m2 oral twice daily, Days 1 - 14 and Bevacizumab 7.5 mg/kg IV over 90 minutes on Day 1 and Oxaliplatin 130 mg/m2 IV over 2 hours Day 1 of 21-day cycle.
- id
- FG000
- title
- Bevacizumab + Capecitabine + Oxaliplatin
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 30
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 28
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- August 2011 to November 2014. All recruitment done at The University of Texas MD Anderson Cancer Center.
Complete source fields
- groups
- description
- Capecitabine 750 mg/m2 oral twice daily, Days 1 - 14 and Bevacizumab 7.5 mg/kg IV over 90 minutes on Day 1 and Oxaliplatin 130 mg/m2 IV over 2 hours Day 1 of 21-day cycle.
- id
- FG000
- title
- Bevacizumab + Capecitabine + Oxaliplatin
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 30
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 28
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- August 2011 to November 2014. All recruitment done at The University of Texas MD Anderson Cancer Center.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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