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:
EG003
Title:
Arm IV (Olaparib) (Phase II Only)
Description:
Patients receive olaparib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT and MRI throughout the study. (In July 2018, the Data Monitoring Committee voted to exclude the olaparib alone regimen).
Computed Tomography: Undergo CT
Magnetic Resonance Imaging: Undergo MRI
Olaparib: Given PO
Questionnaire Administration: Ancillary studies
Deaths Number Affected:
45
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
49
Other Number Affected:
46
Other Number At Risk:
49
Study:
NCT02502266
Results Section:
NCT02502266
Adverse Events Module:
NCT02502266