NCT00352105 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients undergo hyperfractionated radiotherapy twice daily, 5 days a week, beginning on day 1 and continuing for 6 weeks. Patients also receive fluorouracil IN continuously over 96 hrs. and cisplatin IV continuously over 96 hrs. on days 1-3 and 22-25 and oral gefitinib beginning once daily on day 1 and continuing for up to 2 years in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- 5-FU, Cisplatin, Radiation and Iressa
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 19
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Protocol Violation
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 60
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 20
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 40
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- Patients accrued between April 2003 and December 2007 from clinical facility
Complete source fields
- groups
- description
- Patients undergo hyperfractionated radiotherapy twice daily, 5 days a week, beginning on day 1 and continuing for 6 weeks. Patients also receive fluorouracil IN continuously over 96 hrs. and cisplatin IV continuously over 96 hrs. on days 1-3 and 22-25 and oral gefitinib beginning once daily on day 1 and continuing for up to 2 years in the absence of disease progression or unacceptable toxicity.
- id
- FG000
- title
- 5-FU, Cisplatin, Radiation and Iressa
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 9
- type
- Lack of Efficacy
- reasons
- group Id
- FG000
- num Subjects
- 19
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Protocol Violation
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 60
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 20
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 40
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- Patients accrued between April 2003 and December 2007 from clinical facility
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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