NCT00581919 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Bortezomib 1.3 mg/m2 IV days 1, 4, 8, and 11 Dexamethasone 20 mg PO days 1, 4, 8, and 11 Doxorubicin 15 mg/m2 IV days 1 and 8 Acetyl-L-Carnitine (ALCAR) 1.5 g PO BID days 1-21 Maximum of 8 cycles. Each cycle is 21 days long
- id
- FG000
- title
- Bort, Dex, and Dox With ALCAR
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 8
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 10
- type
- Disease Progression
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Other Complicating Disease
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Started Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 32
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 24
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- No events between enrollment and group assignment. All subjects are enrolled are assigned to the same group.
- recruitment Details
- Participants were recruited from University of Wisconsin Hospital and Clinics and the Wisconsin Oncology Network between April 2004 and September 2010.
Complete source fields
- groups
- description
- Bortezomib 1.3 mg/m2 IV days 1, 4, 8, and 11 Dexamethasone 20 mg PO days 1, 4, 8, and 11 Doxorubicin 15 mg/m2 IV days 1 and 8 Acetyl-L-Carnitine (ALCAR) 1.5 g PO BID days 1-21 Maximum of 8 cycles. Each cycle is 21 days long
- id
- FG000
- title
- Bort, Dex, and Dox With ALCAR
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 8
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 10
- type
- Disease Progression
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Other Complicating Disease
- reasons
- group Id
- FG000
- num Subjects
- 2
- type
- Started Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Withdrawal by Subject
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 32
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 8
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 24
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- No events between enrollment and group assignment. All subjects are enrolled are assigned to the same group.
- recruitment Details
- Participants were recruited from University of Wisconsin Hospital and Clinics and the Wisconsin Oncology Network between April 2004 and September 2010.
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Preserved source evidence · Not medical advice
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