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 @ 5:00 PM
Ignite Modification Date:
2025-12-25 @ 2:41 PM
NCT ID:
NCT01169350
Group ID:
EG000
Title:
Diagnostic (18F FDG and 18F FMISO PET/CT)
Description:
Patients undergo 18F FDG and 18F FMISO PET/CT scans before starting neoadjuvant chemotherapy (without or without radiotherapy) and after completion of 4 courses of neoadjuvant therapy.
fludeoxyglucose F 18: Undergo 18F FDG and 18F FMISO PET/CT scans
18F-fluoromisonidazole: Undergo 18F FDG and 18F FMISO PET/CT scans
positron emission tomography: Undergo 18F FDG and 18F FMISO PET/CT scans
computed tomography: Undergo 18F FDG and 18F FMISO PET/CT scans
laboratory biomarker analysis: Correlative studies
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
8
Other Number Affected:
0
Other Number At Risk:
8
Study:
NCT01169350
Results Section:
NCT01169350
Adverse Events Module:
NCT01169350