NCT00738530 · 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
- 327
- group Id
- BG001
- value
- 322
- group Id
- BG002
- value
- 649
- units
- Participants
- groups
- description
- Bevacizumab infusions were administered every two weeks at a dose of 10 mg/kg for 52 weeks or until disease progression or unacceptable toxicity. IFN-Alfa-2A was administered 3 times per week as a subcutaneous injection at a dose of 9 MIU for 52 weeks or until disease progression or major toxicity.
- id
- BG000
- title
- Bevacizumab + IFN-Alfa-2A
- description
- Placebo matched with Bevacizumab infusions were administered every two weeks for 52 weeks or until disease progression or unacceptable toxicity. IFN-Alfa-2A was administered 3 times per week as a subcutaneous injection at a dose of 9 MIU for 52 weeks or until disease progression or major toxicity.
- id
- BG001
- title
- Placebo + IFN-Alfa-2A
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 10.12
- value
- 60.1
- group Id
- BG001
- spread
- 10.89
- value
- 59.4
- group Id
- BG002
- spread
- 10.51
- value
- 59.7
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 105
- group Id
- BG001
- value
- 87
- group Id
- BG002
- value
- 192
- title
- Female
- measurements
- group Id
- BG000
- value
- 222
- group Id
- BG001
- value
- 235
- group Id
- BG002
- value
- 457
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- population Description
- Intent-to-treat population (ITT) included all participants randomized into the study.
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 327
- group Id
- BG001
- value
- 322
- group Id
- BG002
- value
- 649
- units
- Participants
- groups
- description
- Bevacizumab infusions were administered every two weeks at a dose of 10 mg/kg for 52 weeks or until disease progression or unacceptable toxicity. IFN-Alfa-2A was administered 3 times per week as a subcutaneous injection at a dose of 9 MIU for 52 weeks or until disease progression or major toxicity.
- id
- BG000
- title
- Bevacizumab + IFN-Alfa-2A
- description
- Placebo matched with Bevacizumab infusions were administered every two weeks for 52 weeks or until disease progression or unacceptable toxicity. IFN-Alfa-2A was administered 3 times per week as a subcutaneous injection at a dose of 9 MIU for 52 weeks or until disease progression or major toxicity.
- id
- BG001
- title
- Placebo + IFN-Alfa-2A
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 10.12
- value
- 60.1
- group Id
- BG001
- spread
- 10.89
- value
- 59.4
- group Id
- BG002
- spread
- 10.51
- value
- 59.7
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 105
- group Id
- BG001
- value
- 87
- group Id
- BG002
- value
- 192
- title
- Female
- measurements
- group Id
- BG000
- value
- 222
- group Id
- BG001
- value
- 235
- group Id
- BG002
- value
- 457
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- population Description
- Intent-to-treat population (ITT) included all participants randomized into the study.
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Preserved source evidence · Not medical advice
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