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 @ 3:47 AM
Ignite Modification Date:
2025-12-26 @ 2:35 AM
NCT ID:
NCT01367002
Group ID:
EG000
Title:
Carboplatin/Paclitaxel
Description:
Chemotherapy
Carboplatin/Paclitaxel: Paclitaxel 175 mg/m2 will administered intravenously every 21 days for 6 cycles. Carboplatin AUC 5 will be administered intravenously every 21 days for 6 cycles. 100% of patients will receive Carboplatin/Paclitaxel.
Deaths Number Affected:
21
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
28
Other Number Affected:
28
Other Number At Risk:
28
Study:
NCT01367002
Results Section:
NCT01367002
Adverse Events Module:
NCT01367002