NCT01557881 · 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
- At time of scan. No more than 24 hours.
- Other-event reporting threshold
- 5%
No adverse events were documented for this study
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Diagnostic (PET/MRI) | 0 / 98 | 0 / 98 | Not reported / Not reported |
Serious adverse events
Other reported adverse events
Complete source fields
- description
- No adverse events were documented for this study
- event Groups
- description
- After undergoing standard PET/CT, patients undergo PET/MRI. magnetic resonance imaging with positron emission tomography scanning: University Hospitals Seidman Cancer Center \[SCC\] will house the Philips Ingenuity TF PET/MR, which is a hybrid scanner that merges magnetic resonance imaging with positron emission tomography scanning. University Hospitals is one of only five hospitals in the world with this technology. The PET/MRI system consists of two imaging scanners used sequentially as in PET/CT. The 3Tesla MRI component provides the high resolution that is necessary for soft tissue contrast and functional information on perfusion, diffusion, or metabolism. PET provides information about cellular metabolism and receptor status.
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 98
- serious Num Affected
- 0
- serious Num At Risk
- 98
- title
- Diagnostic (PET/MRI)
- frequency Threshold
- 5
- time Frame
- At time of scan. No more than 24 hours.
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
Triangle