NCT00282087 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Gemcitabine 900 mg/m2 on days 1 and 8 intravenously over 90 minutes, followed by Docetaxel 75 mg/m2 on day 8 intravenously over 1 hour.
- id
- FG000
- title
- Women Treated With Adjuvant Regimen for High Risk Uterine LMS
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 47
- type
- STARTED
- achievements
- comment
- One patient died during cycle 1 of treatment because of infectious complications of AIDS.
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 1
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- This was multi-center study open at 11 major medical centers across the United States.
Complete source fields
- groups
- description
- Gemcitabine 900 mg/m2 on days 1 and 8 intravenously over 90 minutes, followed by Docetaxel 75 mg/m2 on day 8 intravenously over 1 hour.
- id
- FG000
- title
- Women Treated With Adjuvant Regimen for High Risk Uterine LMS
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 47
- type
- STARTED
- achievements
- comment
- One patient died during cycle 1 of treatment because of infectious complications of AIDS.
- group Id
- FG000
- num Subjects
- 46
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 1
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- This was multi-center study open at 11 major medical centers across the United States.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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