NCT01772719 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Simvastatin and zoledronic acid: 1. Simvastatin 80 mg PO daily starting two days before starting chemotherapy and stopping two days after chemotherapy. 2. Zoledronic acid 4 mg IV over 15 minutes on day 1 and then monthly.
- id
- FG000
- title
- Simvastatin and Zoledronic Acid
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Lost to Follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- 7 subjects were enrolled into this trial by the investigator from medical clinic
Complete source fields
- groups
- description
- Simvastatin and zoledronic acid: 1. Simvastatin 80 mg PO daily starting two days before starting chemotherapy and stopping two days after chemotherapy. 2. Zoledronic acid 4 mg IV over 15 minutes on day 1 and then monthly.
- id
- FG000
- title
- Simvastatin and Zoledronic Acid
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Lost to Follow-up
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 7
- type
- NOT COMPLETED
- title
- Overall Study
- recruitment Details
- 7 subjects were enrolled into this trial by the investigator from medical clinic
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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