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 @ 3:07 PM
Ignite Modification Date:
2025-12-25 @ 1:28 PM
NCT ID:
NCT03680092
Group ID:
EG001
Title:
Methotrexate and Tacrolimus
Description:
The GVHD prophylaxis regimen on the standard of care arm will consist of methotrexate on Days +1,+3, +6 and +11 and tacrolimus
Methotrexate: standard of care Methotrexate 5 mg/m2 on Days 1, 3, 6 and 11
Tacrolimus: Tacrolimus per institutional guidelines
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
15
Other Number Affected:
10
Other Number At Risk:
15
Study:
NCT03680092
Results Section:
NCT03680092
Adverse Events Module:
NCT03680092