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 @ 4:33 PM
Ignite Modification Date:
2025-12-25 @ 2:25 PM
NCT ID:
NCT02502266
Group ID:
EG002
Title:
Arm III (Cediranib Maleate)
Description:
Patients receive cediranib maleate PO daily continuously. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT and MRI throughout the study.
Cediranib: Given PO
Cediranib Maleate: Given PO
Computed Tomography: Undergo CT
Magnetic Resonance Imaging: Undergo MRI
Questionnaire Administration: Ancillary studies
Deaths Number Affected:
143
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
162
Other Number Affected:
162
Other Number At Risk:
162
Study:
NCT02502266
Results Section:
NCT02502266
Adverse Events Module:
NCT02502266