NCT03951220 · OUTCOME
Primary Outcome 2: Quantifying Bone Loss - Inter-Group Differences in Baseline Serum Sclerostin
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- picogram per litre
- Interval / dispersion
- Standard Deviation
- Time frame
- At baseline
What was measured
Primary Outcome 2: To assess whether the novel magnetic resonance (MR) protocol and exploratory bone turnover markers can improve quantification of bone loss in patients with myeloma (new, relapsed, smouldering) and Monoclonal Gammopathy Of Uncertain Significance (MGUS) at baseline assessment, compared to Dual-energy X-ray Absorptiometry (DXA) and established bone turnover markers alone. This particular section analysed the inter-group difference in baseline serum sclerostin bone turnover marker levels, in patients from Groups 1a (new myeloma), 1b (relapsed myeloma), 1c (smouldering myeloma) and 2 (MGUS).
Analysis population: All participants recruited at baseline from Groups 1 and 2 who had successful measurement of baseline serum sclerostin.
Groups in this outcome
Group 1a: New Myeloma
Cohort of patients recruited as new myeloma at baseline
Group 1b: Relapsed Myeloma
Cohort of patients recruited as relapsed myeloma at baseline
Group 1c: Smouldering Myeloma
Cohort of patients recruited as smouldering myeloma at baseline
Group 2: MGUS
Cohort of patients recruited as MGUS at baseline
| Group | Source count |
|---|---|
| Group 1a: New Myeloma | 14 |
| Group 1b: Relapsed Myeloma | 12 |
| Group 1c: Smouldering Myeloma | 15 |
| Group 2: MGUS | 14 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Group 1a: New Myeloma | 168.5 | 84.1 | Not reported | Not reported | Not reported |
| Group 1b: Relapsed Myeloma | 165.5 | 85.1 | Not reported | Not reported | Not reported |
| Group 1c: Smouldering Myeloma | 166.9 | 86.9 | Not reported | Not reported | Not reported |
| Group 2: MGUS | 164.9 | 83.6 | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 84.1
- value
- 168.5
- group Id
- OG001
- spread
- 85.1
- value
- 165.5
- group Id
- OG002
- spread
- 86.9
- value
- 166.9
- group Id
- OG003
- spread
- 83.6
- value
- 164.9
- denoms
- counts
- group Id
- OG000
- value
- 14
- group Id
- OG001
- value
- 12
- group Id
- OG002
- value
- 15
- group Id
- OG003
- value
- 14
- units
- Participants
- description
- Primary Outcome 2: To assess whether the novel magnetic resonance (MR) protocol and exploratory bone turnover markers can improve quantification of bone loss in patients with myeloma (new, relapsed, smouldering) and Monoclonal Gammopathy Of Uncertain Significance (MGUS) at baseline assessment, compared to Dual-energy X-ray Absorptiometry (DXA) and established bone turnover markers alone. This particular section analysed the inter-group difference in baseline serum sclerostin bone turnover marker levels, in patients from Groups 1a (new myeloma), 1b (relapsed myeloma), 1c (smouldering myeloma) and 2 (MGUS).
- dispersion Type
- Standard Deviation
- groups
- description
- Cohort of patients recruited as new myeloma at baseline
- id
- OG000
- title
- Group 1a: New Myeloma
- description
- Cohort of patients recruited as relapsed myeloma at baseline
- id
- OG001
- title
- Group 1b: Relapsed Myeloma
- description
- Cohort of patients recruited as smouldering myeloma at baseline
- id
- OG002
- title
- Group 1c: Smouldering Myeloma
- description
- Cohort of patients recruited as MGUS at baseline
- id
- OG003
- title
- Group 2: MGUS
- param Type
- MEAN
- population Description
- All participants recruited at baseline from Groups 1 and 2 who had successful measurement of baseline serum sclerostin.
- reporting Status
- POSTED
- time Frame
- At baseline
- title
- Primary Outcome 2: Quantifying Bone Loss - Inter-Group Differences in Baseline Serum Sclerostin
- type
- PRIMARY
- unit Of Measure
- picogram per litre
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Preserved source evidence · Not medical advice
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