NCT00243074 · OUTCOME
Adverse Event Rates
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
- Daily during protocol treatment
What was measured
Adverse events per the NCI Common Toxicity Criteria version 3.0 that were possibly, probably or definitely related to protocol treatment. See adverse event tables for specific details.
Analysis population: All patients who received protocol treatment were assessed for adverse events. See adverse event tables for specific details.
Groups in this outcome
AZD2171 (Cediranib Maleate)
Not reported
| Group | Source count |
|---|---|
| AZD2171 (Cediranib Maleate) | 47 |
Reported measurements
Source class 1
| Group | Value | Spread | Lower | Upper | Comment |
|---|---|---|---|---|---|
| AZD2171 (Cediranib Maleate) | 47 | Not reported | Not reported | Not reported | Not reported |
Complete source fields
- classes
- categories
- measurements
- group Id
- OG000
- value
- 47
- denoms
- counts
- group Id
- OG000
- value
- 47
- units
- Participants
- description
- Adverse events per the NCI Common Toxicity Criteria version 3.0 that were possibly, probably or definitely related to protocol treatment. See adverse event tables for specific details.
- groups
- id
- OG000
- title
- AZD2171 (Cediranib Maleate)
- param Type
- COUNT_OF_PARTICIPANTS
- population Description
- All patients who received protocol treatment were assessed for adverse events. See adverse event tables for specific details.
- reporting Status
- POSTED
- time Frame
- Daily during protocol treatment
- title
- Adverse Event Rates
- type
- SECONDARY
- unit Of Measure
- Participants
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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