NCT00803062 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG000
- title
- Arm I (Paclitaxel and Cisplatin)
- description
- Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG001
- title
- Arm II (Paclitaxel, Cisplatin, Bevacizumab)
- description
- Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Cycles repeated q21 days to progression/toxicity
- id
- FG002
- title
- Arm III (Topotecan Hydrochloride and Paclitaxel)
- description
- Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG003
- title
- Arm IV (Topotecan Hydrochloride, Paclitaxel, Bevacizumab)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 115
- group Id
- FG002
- num Subjects
- 111
- group Id
- FG003
- num Subjects
- 112
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 115
- group Id
- FG002
- num Subjects
- 111
- group Id
- FG003
- num Subjects
- 112
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 4/6/2009 and closed to accrual on 1/3/2012.
Complete source fields
- groups
- description
- Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG000
- title
- Arm I (Paclitaxel and Cisplatin)
- description
- Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG001
- title
- Arm II (Paclitaxel, Cisplatin, Bevacizumab)
- description
- Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Cycles repeated q21 days to progression/toxicity
- id
- FG002
- title
- Arm III (Topotecan Hydrochloride and Paclitaxel)
- description
- Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
- id
- FG003
- title
- Arm IV (Topotecan Hydrochloride, Paclitaxel, Bevacizumab)
- periods
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 115
- group Id
- FG002
- num Subjects
- 111
- group Id
- FG003
- num Subjects
- 112
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 114
- group Id
- FG001
- num Subjects
- 115
- group Id
- FG002
- num Subjects
- 111
- group Id
- FG003
- num Subjects
- 112
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- group Id
- FG003
- num Subjects
- 0
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- The study was activated on 4/6/2009 and closed to accrual on 1/3/2012.
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
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