NCT00473590 · BASELINE
Baseline characteristics
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- denoms
- counts
- group Id
- BG000
- value
- 53
- group Id
- BG001
- value
- 49
- group Id
- BG002
- value
- 102
- units
- Participants
- groups
- description
- Participants received bortezomib 1.3 mg/m\^2 administered as a 3- to 5-second bolus intravenous injection on Days 1, 4, 8, and 11 of a 21-day cycle for a maximum of eight cycles and placebo intravenous infusion on the first day of each 21-day cycle during the blinded treatment phase. At the completion of the 8-cycle treatment phase, participants entered the observation phase until disease progression.
- id
- BG000
- title
- BORT + P
- description
- Participants received bortezomib 1.3 mg/m\^2 administered as a 3- to 5-second bolus intravenous injection on Days 1, 4, 8, and 11 of a 21-day cycle for a maximum of eight cycles and bevacizumab 15 mg/kg administered by intravenous infusion on the first day of each 21-day cycle during the blinded treatment phase. After completion of 8 cycles, participants could continue to receive bevacizumab as monotherapy until disease progression.
- id
- BG001
- title
- BORT + BV
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.2
- value
- 64.9
- group Id
- BG001
- spread
- 9.3
- value
- 65.6
- group Id
- BG002
- spread
- 9.2
- value
- 65.2
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 23
- group Id
- BG001
- value
- 20
- group Id
- BG002
- value
- 43
- title
- Female
- measurements
- group Id
- BG000
- value
- 30
- group Id
- BG001
- value
- 29
- group Id
- BG002
- value
- 59
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 53
- group Id
- BG001
- value
- 49
- group Id
- BG002
- value
- 102
- units
- Participants
- groups
- description
- Participants received bortezomib 1.3 mg/m\^2 administered as a 3- to 5-second bolus intravenous injection on Days 1, 4, 8, and 11 of a 21-day cycle for a maximum of eight cycles and placebo intravenous infusion on the first day of each 21-day cycle during the blinded treatment phase. At the completion of the 8-cycle treatment phase, participants entered the observation phase until disease progression.
- id
- BG000
- title
- BORT + P
- description
- Participants received bortezomib 1.3 mg/m\^2 administered as a 3- to 5-second bolus intravenous injection on Days 1, 4, 8, and 11 of a 21-day cycle for a maximum of eight cycles and bevacizumab 15 mg/kg administered by intravenous infusion on the first day of each 21-day cycle during the blinded treatment phase. After completion of 8 cycles, participants could continue to receive bevacizumab as monotherapy until disease progression.
- id
- BG001
- title
- BORT + BV
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.2
- value
- 64.9
- group Id
- BG001
- spread
- 9.3
- value
- 65.6
- group Id
- BG002
- spread
- 9.2
- value
- 65.2
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 23
- group Id
- BG001
- value
- 20
- group Id
- BG002
- value
- 43
- title
- Female
- measurements
- group Id
- BG000
- value
- 30
- group Id
- BG001
- value
- 29
- group Id
- BG002
- value
- 59
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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