NCT00740597 · 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%
Only one patients was on treatment for 5 days with no adverse events to report.
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Arm 1 | 0 / 0 | 0 / 0 | Not reported / Not reported |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- Only one patients was on treatment for 5 days with no adverse events to report.
- event Groups
- description
- pre-operative radiation + surgery PTV will receive a total dose of 50 Gy in 25 fractions, 2 Gy per fraction, 5 fractions per week, over approximately 5 weeks. Concurrently, the GTV2, if present, will receive 54 Gy in 25 fraction. Dose will be prescribed to the isodose volume that encompasses the PTV. All patients will be treated by 6 MV photon beam.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 0
- serious Num Affected
- 0
- serious Num At Risk
- 0
- title
- Arm 1
- frequency Threshold
- 0
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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