NCT00594815 · OUTCOME
Total Number of Participants Who Experienced Acute Treatment Related Adverse Events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- COUNT_OF_PARTICIPANTS
- Unit
- Participants
- Interval / dispersion
- Not reported
- Time frame
- 2 years
What was measured
The toxicity of this combined regimen will be measured using the NCI CTC version 2.0.
Groups in this outcome
Immunocompetent Pts With Newly Diagnosed Primary CNS Lymphoma
Cytarabine, Leucovorin, Methotrexate, Procarbazine, Rituximab, Vincristine: Immunochemotherapy
| Group | Source count |
|---|---|
| Immunocompetent Pts With Newly Diagnosed Primary CNS Lymphoma | 52 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Immunocompetent Pts With Newly Diagnosed Primary CNS Lymphoma | 52 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 52
- denoms
- counts
- group Id
- OG000
- value
- 52
- units
- Participants
- description
- The toxicity of this combined regimen will be measured using the NCI CTC version 2.0.
- groups
- description
- Cytarabine, Leucovorin, Methotrexate, Procarbazine, Rituximab, Vincristine: Immunochemotherapy
- id
- OG000
- title
- Immunocompetent Pts With Newly Diagnosed Primary CNS Lymphoma
- param Type
- COUNT_OF_PARTICIPANTS
- reporting Status
- POSTED
- time Frame
- 2 years
- title
- Total Number of Participants Who Experienced Acute Treatment Related Adverse Events
- type
- PRIMARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle