NCT00942331 · 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 gemcitabine hydrochloride and cisplatin as in arm I. Patients also receive bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 21 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients then receive bevacizumab IV over 30-90 minutes every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Arm II (GCB)
- description
- Patients receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8 and cisplatin IV and placebo IV over 30-90 minutes on day 1. Treatment repeats every 21 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients then receive placebo IV over 30-90 minutes every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG001
- title
- Arm I (GCP)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 22
- type
- Did not start treatment
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 252
- group Id
- FG001
- num Subjects
- 254
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 237
- group Id
- FG001
- num Subjects
- 232
- comment
- Started treatment
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 22
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Patients receive gemcitabine hydrochloride and cisplatin as in arm I. Patients also receive bevacizumab IV over 30-90 minutes on day 1. Treatment repeats every 21 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients then receive bevacizumab IV over 30-90 minutes every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- Arm II (GCB)
- description
- Patients receive gemcitabine hydrochloride IV over 30 minutes on days 1 and 8 and cisplatin IV and placebo IV over 30-90 minutes on day 1. Treatment repeats every 21 days for 6 cycles in the absence of disease progression or unacceptable toxicity. Patients then receive placebo IV over 30-90 minutes every 21 days in the absence of disease progression or unacceptable toxicity.
- id
- FG001
- title
- Arm I (GCP)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 22
- type
- Did not start treatment
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 252
- group Id
- FG001
- num Subjects
- 254
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 237
- group Id
- FG001
- num Subjects
- 232
- comment
- Started treatment
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 22
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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