NCT02130427 · 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
- Adverse events were not collected for this imaging trial.
- Other-event reporting threshold
- 0%
Adverse events were not collected for this imaging trial as they would not be relevant to the purposes of the trial (to track change in GTV over time via CT scans).
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Complete Imaging | 0 / 0 | 0 / 0 | 0 / 0 |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Adverse events were not collected for this imaging trial as they would not be relevant to the purposes of the trial (to track change in GTV over time via CT scans).
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 0
- description
- Weekly 3D/4D CT scans during radiation therapy. MRI may be used in addition to or instead of CT depending on the location of the tumor and the decision of the treating physician. CT scan: Weekly 3D/4D CT scan
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Complete Imaging
- frequency Threshold
- 0
- time Frame
- Adverse events were not collected for this imaging trial.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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