NCT03109262 · 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
- 0%
| Safety group | Serious events | Other events | Deaths |
|---|---|---|---|
| Yttrium Y-90 PET/CT vs 99mTc-MAA SPECT/CT Scans | 0 / 42 | 0 / 42 | 0 / 42 |
Serious adverse events
Other reported adverse events
Complete source fields
- event Groups
- deaths Num Affected
- 0
- deaths Num At Risk
- 42
- description
- All participants receive both Y-90 PET/CT vs 99mTc-MAA SPECT/CT Scans * Computed Tomography (CT): As part of PET/CT and SPECT/CT scans. * Positron Emission Tomography (PET): As part of PET/CT scan * Single-photon emission computerized tomography (SPECT) scan: As part of SPECT/CT scan * 90-Yttrium (Y-90) Glass Microspheres: Radiolabel for PET/CT scan * Technetium 99mTc albumin aggregated (99mTc-MAA): Radiolabel for 99mTc-MAA SPECT/CT Scan
- id
- EG000
- other Num Affected
- 0
- other Num At Risk
- 42
- serious Num Affected
- 0
- serious Num At Risk
- 42
- title
- Yttrium Y-90 PET/CT vs 99mTc-MAA SPECT/CT Scans
- frequency Threshold
- 0
- time Frame
- 1 day
Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f
Preserved source evidence · Not medical advice
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