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 @ 2:23 PM
Ignite Modification Date:
2025-12-25 @ 12:59 PM
NCT ID:
NCT03141359
Group ID:
EG000
Title:
SBRT + Concurrent Mediastinal Chemoradiation +/- Consolidation Chemotherapy/Adjuvant Immunotherapy
Description:
SBRT + Concurrent Mediastinal Chemoradiation +/- Consolidation Chemotherapy/Adjuvant Immunotherapy
SBRT: Primary tumor stereotactic body radiation therapy (SBRT)
Concurrent chemotherapy: (Carboplatin + Paclitaxel) or (cis Platinum + Etoposide)
Mediastinal radiation: intensity-modulated radiation therapy (IMRT)
Adjuvant immunotherapy: durvalumab
Deaths Number Affected:
32
Deaths Number At Risk:
None
Serious Number Affected:
23
Serious Number At Risk:
61
Other Number Affected:
61
Other Number At Risk:
61
Study:
NCT03141359
Results Section:
NCT03141359
Adverse Events Module:
NCT03141359