NCT01314963 · 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
- 1 day
- Other-event reporting threshold
- 5%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| All Participants - Intraoperative Handheld Gamma Camera (pIHGC | 0 / 50 | 0 / 50 | 0 / 50 |
| All Participants - Gamma Probes (GP) | 0 / 50 | 0 / 50 | 0 / 50 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 50
- description
- The entire set of sentinel lymph nodes (SLNs) excised from study participants (ie, all participants) were evaluated with the intraoperative handheld gamma camera (pIHGC).
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 50
- serious Num Affected
- 0
- serious Num At Risk
- 50
- title
- All Participants - Intraoperative Handheld Gamma Camera (pIHGC
- deaths Num Affected
- 0
- deaths Num At Risk
- 50
- description
- The entire set of sentinel lymph nodes (SLNs) excised from study participants (ie, all participants) were evaluated with the gamma probes (GP).
- id
- EG001
- other Num Affected
- 0
- other Num At Risk
- 50
- serious Num Affected
- 0
- serious Num At Risk
- 50
- title
- All Participants - Gamma Probes (GP)
- frequency Threshold
- 5
- time Frame
- 1 day
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle