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 @ 11:48 AM
Ignite Modification Date:
2025-12-26 @ 10:20 AM
NCT ID:
NCT05736861
Group ID:
EG001
Title:
Arm A - Placebo
Description:
Placebo - appearance and size matched to active study drug.
Participant will be instructed to take a pre-specified number of tablets for 3 consecutive days based on their weight, matched to active study drug dosing.
Placebo: Each study arm will contain a placebo comparator. Placebo will look similar to study drug and will be administered via the same route of administration and dose. However, placebo will be an inactive substance, containing no study drug.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
774
Other Number Affected:
13
Other Number At Risk:
774
Study:
NCT05736861
Results Section:
NCT05736861
Adverse Events Module:
NCT05736861