NCT02041325 · 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
- 22
- group Id
- BG001
- value
- 16
- group Id
- BG002
- value
- 38
- units
- Participants
- groups
- description
- Subjects will receive oral CC-5013 (lenalidomide) at 25 mg qd for 7 days prior to and 7 days after the vaccine.
- id
- BG000
- title
- Lenalidomide
- description
- Subjects will receive placebo for 7 days prior to and 7 days after the vaccine.
- id
- BG001
- title
- Placebo
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- lower Limit
- 46
- upper Limit
- 90
- value
- 77
- group Id
- BG001
- lower Limit
- 47
- upper Limit
- 78
- value
- 67.5
- group Id
- BG002
- lower Limit
- 46
- upper Limit
- 90
- value
- 72.3
- dispersion Type
- FULL_RANGE
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 5
- group Id
- BG001
- value
- 6
- group Id
- BG002
- value
- 11
- title
- Female
- measurements
- group Id
- BG000
- value
- 17
- group Id
- BG001
- value
- 10
- group Id
- BG002
- value
- 27
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- classes
- categories
- measurements
- group Id
- BG000
- value
- 22
- group Id
- BG001
- value
- 16
- group Id
- BG002
- value
- 38
- title
- United States
- param Type
- NUMBER
- title
- Region of Enrollment
- unit Of Measure
- Participants
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 22
- group Id
- BG001
- value
- 16
- group Id
- BG002
- value
- 38
- units
- Participants
- groups
- description
- Subjects will receive oral CC-5013 (lenalidomide) at 25 mg qd for 7 days prior to and 7 days after the vaccine.
- id
- BG000
- title
- Lenalidomide
- description
- Subjects will receive placebo for 7 days prior to and 7 days after the vaccine.
- id
- BG001
- title
- Placebo
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- lower Limit
- 46
- upper Limit
- 90
- value
- 77
- group Id
- BG001
- lower Limit
- 47
- upper Limit
- 78
- value
- 67.5
- group Id
- BG002
- lower Limit
- 46
- upper Limit
- 90
- value
- 72.3
- dispersion Type
- FULL_RANGE
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 5
- group Id
- BG001
- value
- 6
- group Id
- BG002
- value
- 11
- title
- Female
- measurements
- group Id
- BG000
- value
- 17
- group Id
- BG001
- value
- 10
- group Id
- BG002
- value
- 27
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- classes
- categories
- measurements
- group Id
- BG000
- value
- 22
- group Id
- BG001
- value
- 16
- group Id
- BG002
- value
- 38
- title
- United States
- param Type
- NUMBER
- title
- Region of Enrollment
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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