NCT00423930 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- This is a single-institution phase II study. The primary endpoint is to determine 2-year progression-free survival for patients with locally or regionally advanced HNSCC treated with concurrent intensity modulated radiation therapy (IMRT) + cisplatin + bevacizumab. bevacizumab cisplatin conventional surgery intensity-modulated radiation therapy
- id
- FG000
- title
- IMRT + Cisplatin + Bevacizumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 44
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 42
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- This is a single-institution phase II study. The primary endpoint is to determine 2-year progression-free survival for patients with locally or regionally advanced HNSCC treated with concurrent intensity modulated radiation therapy (IMRT) + cisplatin + bevacizumab. bevacizumab cisplatin conventional surgery intensity-modulated radiation therapy
- id
- FG000
- title
- IMRT + Cisplatin + Bevacizumab
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 44
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 42
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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