Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 2:31 PM
Ignite Modification Date:
2025-12-25 @ 1:04 PM
NCT ID:
NCT04252859
Group ID:
EG000
Title:
Pilot Phase
Description:
Subjects with biopsy-proven invasive lobular carcinoma (ILC), diagnosed within 12 weeks of imaging, will undergo one 18F-Fluoroestradiol (FES) PET/CT scan and one optional 18F-FDG PET/CT(if a standard of care scan not already performed).
For the FES scan, patients are administered a dose of approximately 6 mCi and imaged approximately 60 minutes after injection.
For the FDG scan, patients are administered a dose of approximately 15 mCi and imaged approximately 60 minutes after injection.
\[18F\]Fluoroestradiol (FES) PET/CT: \[18F\]Fluoroestradiol (FES) PET/CT for invasive lobular carcinoma (ILC)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
17
Other Number Affected:
7
Other Number At Risk:
17
Study:
NCT04252859
Results Section:
NCT04252859
Adverse Events Module:
NCT04252859