NCT01586104 · 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
- Not reported
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Treatment (IMRT) | 2 / 20 | 0 / 20 | 2 / 20 |
Serious adverse events
- notes
- Multi-organ failure from progressive and terminal cancer.
- organ System
- General disorders
- stats
- group Id
- EG000
- num Affected
- 2
- num At Risk
- 20
- num Events
- 2
- term
- Deceased from progressive disease.
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 2
- deaths Num At Risk
- 20
- description
- Patients undergo cardiac-sparing whole lung intensity-modulated radiation therapy (IMRT).
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 20
- serious Num Affected
- 2
- serious Num At Risk
- 20
- title
- Treatment (IMRT)
- frequency Threshold
- 0
- serious Events
- notes
- Multi-organ failure from progressive and terminal cancer.
- organ System
- General disorders
- stats
- group Id
- EG000
- num Affected
- 2
- num At Risk
- 20
- num Events
- 2
- term
- Deceased from progressive disease.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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