NCT00749892 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Erlotinib 150 mg by mouth daily for 3 weeks followed by cystectomy within 24 hours of the last dose.
- id
- FG000
- title
- Pre-surgical Erlotinib Treatment
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 34
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 31
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Erlotinib treatment milestone: Three participants decided to not start the study medication.
- recruitment Details
- Recruitment began 6/9/2008 and concluded on 12/19/2011 in the medical clinic. Diagnosis of invasive transitional cell carcinoma in the bladder, upper tract or urethra tumors were required for participants who were candidates for cystectomy to be considered. Participants with high-risk features were generally excluded.
Complete source fields
- groups
- description
- Erlotinib 150 mg by mouth daily for 3 weeks followed by cystectomy within 24 hours of the last dose.
- id
- FG000
- title
- Pre-surgical Erlotinib Treatment
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 34
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 31
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 3
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- Erlotinib treatment milestone: Three participants decided to not start the study medication.
- recruitment Details
- Recruitment began 6/9/2008 and concluded on 12/19/2011 in the medical clinic. Diagnosis of invasive transitional cell carcinoma in the bladder, upper tract or urethra tumors were required for participants who were candidates for cystectomy to be considered. Participants with high-risk features were generally excluded.
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Preserved source evidence · Not medical advice
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