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 @ 5:09 PM
Ignite Modification Date:
2025-12-25 @ 2:47 PM
NCT ID:
NCT02616250
Group ID:
EG000
Title:
Brimonidine 0.33% Gel / CD07805/47 (Br) + Ivermectin 1% Cream
Description:
Half group will receive once-daily Br 0.33% gel in the morning and once-daily IVM 1% cream in the evening for 12 weeks.
Half group will receive once-daily Br vehicle gel in the morning for the first 4 weeks and once-daily Br 0.33% gel in the morning for the following 8 weeks and once-daily IVM 1% cream in the evening for 12 weeks.
Brimonidine 0.33% gel (Br)
CD07805/47 (Br) placebo gel
Ivermectin 1% cream (IVM)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
95
Other Number Affected:
8
Other Number At Risk:
95
Study:
NCT02616250
Results Section:
NCT02616250
Adverse Events Module:
NCT02616250