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 @ 4:19 AM
Ignite Modification Date:
2025-12-26 @ 3:20 AM
NCT ID:
NCT02626520
Group ID:
EG001
Title:
Locally Advanced
Description:
Systemic chemotherapy followed by chemoradiation, followed by definitive surgery
Gemcitabine and nanoparticle albumin bound paclitaxel: Gemcitabine and nab-paclitaxel given every 14 days x 4 cycles
5-fluorouracil and irinotecan: FOLFIRI.3 given every 14 days x 4 cycles
Preoperative chemoradiation: Pre-operative chemoradiation to 40 Gy in 20 fractions
Definitive resection: Definitive surgical resection of primary tumor
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
10
Other Number Affected:
2
Other Number At Risk:
10
Study:
NCT02626520
Results Section:
NCT02626520
Adverse Events Module:
NCT02626520