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 @ 10:52 PM
Ignite Modification Date:
2025-12-25 @ 8:21 PM
NCT ID:
NCT00036569
Group ID:
EG000
Title:
Interferon Alfa
Description:
0.3 mg/kg subcutaneously once a week for 4 weeks beginning 2-10 weeks after completion of radiation therapy and continued until disease progression or one of the other off study criteria.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
32
Serious Number At Risk:
32
Other Number Affected:
32
Other Number At Risk:
32
Study:
NCT00036569
Results Section:
NCT00036569
Adverse Events Module:
NCT00036569