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 @ 10:35 PM
Ignite Modification Date:
2025-12-25 @ 8:07 PM
NCT ID:
NCT01972035
Group ID:
EG000
Title:
ValAcyclovir
Description:
Kidney recipients who give informed consent will be randomly assigned to receive ValA or ValG in a 1:1 ratio. Duration of therapy is 3-12 months depending on risk and age of recipient. Dosing is based on glomerular filtration rate.
Valacyclovir: Experimental Arm
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
52
Serious Number At Risk:
66
Other Number Affected:
64
Other Number At Risk:
66
Study:
NCT01972035
Results Section:
NCT01972035
Adverse Events Module:
NCT01972035