NCT01401907 · ADVERSE EVENTS
Adverse events
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
Adverse events occurred during the study; they are not necessarily caused by treatment. Serious events are not interchangeable with severe/grade 3–4 events. These safety populations may differ from efficacy populations.
- Collection time frame
- 6 months
- Other-event reporting threshold
- 5%
no AE from this non-medication/treatment study
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Early Palliative Care | 0 / 175 | 0 / 175 | 27 / 175 |
| Standard of Care | 0 / 175 | 0 / 175 | 32 / 175 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- no AE from this non-medication/treatment study
- event Groups
- deaths Num Affected
- 27
- deaths Num At Risk
- 175
- description
- Subjects receive standard of care with early palliative care. early palliative care: patient assigned to the intervention will receive early palliative care along with standard oncology care.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 175
- serious Num Affected
- 0
- serious Num At Risk
- 175
- title
- Early Palliative Care
- deaths Num Affected
- 32
- deaths Num At Risk
- 175
- description
- Subjects receives standard of care
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 175
- serious Num Affected
- 0
- serious Num At Risk
- 175
- title
- Standard of Care
- frequency Threshold
- 5
- time Frame
- 6 months
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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