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:
EG000
Title:
Arm A - Ivermectin 400
Description:
Ivermectin - 7-mg tablets
Participant will be instructed to take a pre-specified number of tablets for 3 consecutive days based on their weight for a daily dose of approximately 300-400 µg/kg.
Ivermectin: Each participant will receive a sufficient quantity of 7-mg tablets to be taken as directed based on their weight. The tablets are white, round, biconvex tablets with "123" over the scoring on one side. All packaging will be labeled to indicate that the product is for investigational use.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
817
Other Number Affected:
16
Other Number At Risk:
817
Study:
NCT05736861
Results Section:
NCT05736861
Adverse Events Module:
NCT05736861