NCT01283542 · OUTCOME
Tumor Volume Main Phase (FAS)
Evaluate the Efficacy and Safety of Pasireotide LAR (Long Acting Release) on the Treatment of Patients With Clinically Non-Functioning Pituitary Adenoma. · Source last updated 2019-04-26
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- MEAN
- Unit
- cm^3
- Interval / dispersion
- Standard Deviation
- Time frame
- baseline to week 4, 12, 24
What was measured
Tumor volume was evaluated by MRI. MRIs were performed and processed according to the guidelines of the central evaluator's facility. The pituitary adenomas were measured by a neuro-radiologist, using manual tracing together with the imaging analysis software. The largest diameter at any plan determined the maximum diameter of the tumor.
Analysis population: number of participants with evaluable data varied across visits
Groups in this outcome
Pasireotide LAR
All patients will receive pasireotide LAR (long acting release) 60 mg every 28 ± 3 days for 24 weeks
Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.
Analysis denominator · Participants
| Group | Source count |
|---|
| Pasireotide LAR | 20 |
|---|
Reported measurements
Main Baseline
Analysis denominator · Participants
| Group | Source count |
|---|
| Pasireotide LAR | 20 |
|---|
Values in cm^3 · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Pasireotide LAR | 2.97 | 2.53 | Not reported | Not reported | Not reported |
|---|
Main Week 4
Analysis denominator · Participants
| Group | Source count |
|---|
| Pasireotide LAR | 20 |
|---|
Values in cm^3 · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Pasireotide LAR | 4.31 | 6.66 | Not reported | Not reported | Not reported |
|---|
Main Week 12
Analysis denominator · Participants
| Group | Source count |
|---|
| Pasireotide LAR | 19 |
|---|
Values in cm^3 · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Pasireotide LAR | 4.31 | 6.66 | Not reported | Not reported | Not reported |
|---|
Main Week 24
Analysis denominator · Participants
| Group | Source count |
|---|
| Pasireotide LAR | 20 |
|---|
Values in cm^3 · Interval/dispersion: Standard Deviation| Group | Value | Spread | Lower | Upper | Comment |
|---|
| Pasireotide LAR | 3.39 | 3.15 | Not reported | Not reported | Not reported |
|---|
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- spread
- 2.53
- value
- 2.97
- title
- Main Baseline
- categories
- measurements
- group Id
- OG000
- spread
- 6.66
- value
- 4.31
- title
- Main Week 4
- categories
- measurements
- group Id
- OG000
- spread
- 6.66
- value
- 4.31
- title
- Main Week 12
- categories
- measurements
- group Id
- OG000
- spread
- 3.15
- value
- 3.39
- title
- Main Week 24
- description
- Tumor volume was evaluated by MRI. MRIs were performed and processed according to the guidelines of the central evaluator's facility. The pituitary adenomas were measured by a neuro-radiologist, using manual tracing together with the imaging analysis software. The largest diameter at any plan determined the maximum diameter of the tumor.
- dispersion Type
- Standard Deviation
- groups
- description
- All patients will receive pasireotide LAR (long acting release) 60 mg every 28 ± 3 days for 24 weeks
- id
- OG000
- title
- Pasireotide LAR
- param Type
- MEAN
- population Description
- number of participants with evaluable data varied across visits
- reporting Status
- POSTED
- time Frame
- baseline to week 4, 12, 24
- title
- Tumor Volume Main Phase (FAS)
- type
- SECONDARY
- unit Of Measure
- cm^3
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice