NCT00410605 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive bevacizumab IV over 30-90 minutes on days 1 and 15, oral lenalidomide on days 1-21, and oral dexamethasone on days 1, 8, 15, and 22. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. bevacizumab: Given IV lenalidomide: Given orally dexamethasone: Given orally
- id
- FG000
- title
- Bevacizumab, Dexamethasone, and Lenalidomide
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 12
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Started Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Stopped treatmen to collect stem cells
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Transferred to another Institution
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 14
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- No events between enrollment and group assignment. All subjects enrolled are immediately assigned to Arm 1, "Bevacizumab, Dexamethasone, and Lenalidomide."
- recruitment Details
- Participants were recruited from the University of Wisconsin (UW) Hospital and Clinics, the UW 1 South Park Clinic, and the Wisconsin Oncology Network (WON) clinics between November 2006 and March 2011.
Complete source fields
- groups
- description
- Patients receive bevacizumab IV over 30-90 minutes on days 1 and 15, oral lenalidomide on days 1-21, and oral dexamethasone on days 1, 8, 15, and 22. Courses repeat every 4 weeks in the absence of disease progression or unacceptable toxicity. bevacizumab: Given IV lenalidomide: Given orally dexamethasone: Given orally
- id
- FG000
- title
- Bevacizumab, Dexamethasone, and Lenalidomide
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 12
- type
- Adverse Event
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Physician Decision
- reasons
- group Id
- FG000
- num Subjects
- 5
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- type
- Started Non-Protocol Therapy
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Stopped treatmen to collect stem cells
- reasons
- group Id
- FG000
- num Subjects
- 1
- type
- Transferred to another Institution
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 14
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 25
- type
- NOT COMPLETED
- title
- Overall Study
- pre Assignment Details
- No events between enrollment and group assignment. All subjects enrolled are immediately assigned to Arm 1, "Bevacizumab, Dexamethasone, and Lenalidomide."
- recruitment Details
- Participants were recruited from the University of Wisconsin (UW) Hospital and Clinics, the UW 1 South Park Clinic, and the Wisconsin Oncology Network (WON) clinics between November 2006 and March 2011.
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Preserved source evidence · Not medical advice
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