NCT01055314 · OUTCOME
Feasibility of the Addition of Temozolomide to Chemotherapy Determined by Patient Enrollment
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- Measure
- NUMBER
- Unit
- Proportion of Participants
- Interval / dispersion
- 95% Confidence Interval
- Time frame
- From start to week 26 of therapy
What was measured
Proportion of no Grade 4+ non-hematologic toxicity.
Analysis population: 13 participants were excluded because of ineligibility or insufficient information to assess feasibility.
Groups in this outcome
Temozolomide
Add temozolomide to vincristine/irinotecan cycles.
| Group | Source count |
|---|---|
| Temozolomide | 62 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| Temozolomide | 0.7097 | Not reported | 0.5967 | 0.8227 | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- lower Limit
- 0.5967
- upper Limit
- 0.8227
- value
- 0.7097
- denoms
- counts
- group Id
- OG000
- value
- 62
- units
- Participants
- description
- Proportion of no Grade 4+ non-hematologic toxicity.
- dispersion Type
- 95% Confidence Interval
- groups
- description
- Add temozolomide to vincristine/irinotecan cycles.
- id
- OG000
- title
- Temozolomide
- param Type
- NUMBER
- population Description
- 13 participants were excluded because of ineligibility or insufficient information to assess feasibility.
- reporting Status
- POSTED
- time Frame
- From start to week 26 of therapy
- title
- Feasibility of the Addition of Temozolomide to Chemotherapy Determined by Patient Enrollment
- type
- PRIMARY
- unit Of Measure
- Proportion of Participants
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
Triangle