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:
2025-12-26 @ 10:44 PM
Ignite Modification Date:
2025-12-26 @ 10:44 PM
NCT ID:
NCT02435212
Group ID:
EG001
Title:
DFX DT Cross-over Granule - Optional Extension Phase
Description:
After the Core phase, participants could enter the Optional Extension phase and cross over to DFX granules administered orally once daily in the form of stick packs for up to 5 years. Participants entering the Optional Extension phase received the equivalent strength-adjusted DFX granules dose corresponding to the last DT dose in the Core phase taking dose adjustment guidelines into account.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
22
Serious Number At Risk:
69
Other Number Affected:
63
Other Number At Risk:
69
Study:
NCT02435212
Results Section:
NCT02435212
Adverse Events Module:
NCT02435212