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 @ 12:04 PM
Ignite Modification Date:
2025-12-25 @ 11:58 AM
NCT ID:
NCT01595061
Group ID:
EG000
Title:
GEM+CIS+IMRT
Description:
Gemcitabine 50 mg/m2 and Cisplatin 40mg/m2 administered weekly throughout IMRT radiation therapy. Gemcitabine will be infused prior to cisplatin and given over approximately 30 minutes while the cisplatin will be delivered over approximately 60 minutes.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
24
Serious Number At Risk:
53
Other Number Affected:
53
Other Number At Risk:
53
Study:
NCT01595061
Results Section:
NCT01595061
Adverse Events Module:
NCT01595061