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:
2025-12-25 @ 2:09 AM
Ignite Modification Date:
2025-12-26 @ 12:36 AM
NCT ID:
NCT00227760
Group ID:
EG000
Title:
Treatment (Cediranib Maleate)
Description:
Patients receive cediranib maleate PO QD on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.
Cediranib Maleate: Given PO
Dynamic Contrast-Enhanced Magnetic Resonance Imaging: Correlative studies
Laboratory Biomarker Analysis: Correlative studies
Pharmacological Study: Correlative studies
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
44
Other Number Affected:
2
Other Number At Risk:
44
Study:
NCT00227760
Results Section:
NCT00227760
Adverse Events Module:
NCT00227760