NCT00503997 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive pemetrexed disodium IV and oxaliplatin IV over 2 hours on day 1. Treatment repeats every 14 days for up to 4 courses. If patient progresses before receiving 4 courses of treatment, treatment will be discontinued and patient will proceed to surgery.
- id
- FG000
- title
- Pemetrexed/Oxaliplatin
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- disease progression
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 42
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 34
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- This study consented 42 patients. One patient was found ineligible.
- recruitment Details
- The trial was open to accrual from 12/13/2006 to 4/9/2008.
Complete source fields
- groups
- description
- Patients receive pemetrexed disodium IV and oxaliplatin IV over 2 hours on day 1. Treatment repeats every 14 days for up to 4 courses. If patient progresses before receiving 4 courses of treatment, treatment will be discontinued and patient will proceed to surgery.
- id
- FG000
- title
- Pemetrexed/Oxaliplatin
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- disease progression
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 42
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 34
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- This study consented 42 patients. One patient was found ineligible.
- recruitment Details
- The trial was open to accrual from 12/13/2006 to 4/9/2008.
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Preserved source evidence · Not medical advice
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