NCT00622505 · 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
- 79
- group Id
- BG001
- value
- 42
- group Id
- BG002
- value
- 121
- units
- Participants
- groups
- description
- Participants received 4 mg or a reduced dose, i.e., 3.5 mg, or 3.3 mg or 3.0 mg of Zoledronic acid as an IV infusion over a minimum of 15 minutes every 12 weeks for up to 96 weeks based on the participants most recent urine NTx measurement ( \<50 nmol/mmol creatinine).
- id
- BG000
- title
- Zoledronic Acid Every 12 Weeks
- description
- Participants received 4 mg or a reduced dose, i.e., 3.5 mg, or 3.3 mg or 3.0 mg of Zoledronic acid as an IV infusion over a minimum of 15 minutes every 4 weeks or every 12 weeks for up to 96 weeks based on the participants most recent urine NTx measurement (≥ 50 nmol/mmol creatinine or \<50 nmol/mmol creatinine, respectively).
- id
- BG001
- title
- Zoledronic Acid Every 4 Weeks or 12 Weeks
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.91
- value
- 62.8
- group Id
- BG001
- spread
- 12.66
- value
- 65.8
- group Id
- BG002
- spread
- 10.99
- value
- 63.8
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 36
- group Id
- BG001
- value
- 21
- group Id
- BG002
- value
- 57
- title
- Female
- measurements
- group Id
- BG000
- value
- 43
- group Id
- BG001
- value
- 21
- group Id
- BG002
- value
- 64
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- population Description
- Intent-to-treat (ITT) analysis set included all participants who were enrolled in this study.
Complete source fields
- denoms
- counts
- group Id
- BG000
- value
- 79
- group Id
- BG001
- value
- 42
- group Id
- BG002
- value
- 121
- units
- Participants
- groups
- description
- Participants received 4 mg or a reduced dose, i.e., 3.5 mg, or 3.3 mg or 3.0 mg of Zoledronic acid as an IV infusion over a minimum of 15 minutes every 12 weeks for up to 96 weeks based on the participants most recent urine NTx measurement ( \<50 nmol/mmol creatinine).
- id
- BG000
- title
- Zoledronic Acid Every 12 Weeks
- description
- Participants received 4 mg or a reduced dose, i.e., 3.5 mg, or 3.3 mg or 3.0 mg of Zoledronic acid as an IV infusion over a minimum of 15 minutes every 4 weeks or every 12 weeks for up to 96 weeks based on the participants most recent urine NTx measurement (≥ 50 nmol/mmol creatinine or \<50 nmol/mmol creatinine, respectively).
- id
- BG001
- title
- Zoledronic Acid Every 4 Weeks or 12 Weeks
- description
- Total of all reporting groups
- id
- BG002
- title
- Total
- measures
- classes
- categories
- measurements
- group Id
- BG000
- spread
- 9.91
- value
- 62.8
- group Id
- BG001
- spread
- 12.66
- value
- 65.8
- group Id
- BG002
- spread
- 10.99
- value
- 63.8
- dispersion Type
- STANDARD_DEVIATION
- param Type
- MEAN
- title
- Age, Continuous
- unit Of Measure
- years
- classes
- categories
- measurements
- group Id
- BG000
- value
- 36
- group Id
- BG001
- value
- 21
- group Id
- BG002
- value
- 57
- title
- Female
- measurements
- group Id
- BG000
- value
- 43
- group Id
- BG001
- value
- 21
- group Id
- BG002
- value
- 64
- title
- Male
- param Type
- COUNT_OF_PARTICIPANTS
- title
- Sex: Female, Male
- unit Of Measure
- Participants
- population Description
- Intent-to-treat (ITT) analysis set included all participants who were enrolled in this study.
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Preserved source evidence · Not medical advice
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