NCT02599194 · 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
- 30 days
- Other-event reporting threshold
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| 18F-FSPG and 18F-FDG Intragroup Comparision | 0 / 7 | 1 / 7 | 0 / 7 |
Serious adverse events
Other reported adverse events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (4.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 7
- num Events
- 1
- term
- Elevated blood ammonia
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 7
- description
- Participants sequentially receive radioimaging agents 18F-FSPG and 18F-FDG IV followed by PET/CT scan with 60 minutes. 18F-FSPG: Administered intravenously (IV) 18F-FDG: Administered intravenously (IV)
- id
- EG000
- other Num Affected
- 1
- other Num At Risk
- 7
- serious Num Affected
- 0
- serious Num At Risk
- 7
- title
- 18F-FSPG and 18F-FDG Intragroup Comparision
- frequency Threshold
- 0
- other Events
- assessment Type
- SYSTEMATIC_ASSESSMENT
- organ System
- Metabolism and nutrition disorders
- source Vocabulary
- CTCAE (4.0)
- stats
- group Id
- EG000
- num Affected
- 1
- num At Risk
- 7
- num Events
- 1
- term
- Elevated blood ammonia
- time Frame
- 30 days
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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