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 @ 4:50 PM
Ignite Modification Date:
2025-12-25 @ 2:34 PM
NCT ID:
NCT01905150
Group ID:
EG001
Title:
G-FLIP+VitaminC. When DP Occurred, Then G-FLIP-DM+Vitamin C.
Description:
G-FLIP alone for 2 weeks, then G-FLIP + Vitamin C. When Disease Progression occurred, then G-FLIP-DM + Vitamin C.
G-FLIP: G-FLIP is a combination of Low Doses of Gemcitabine, Fluorouracil \[5FU\], Leucovorin, Irinotecan, and Oxaliplatin
G-FLIP-DM: G-FLIP-DM is low doses of Gemcitabine, Fluorouracil \[5FU\], Leucovorin, Irinotecan, Oxaliplatin, Docetaxel and Mitomycin C
Deaths Number Affected:
18
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
18
Other Number Affected:
13
Other Number At Risk:
18
Study:
NCT01905150
Results Section:
NCT01905150
Adverse Events Module:
NCT01905150