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:
2025-12-25 @ 3:29 AM
Ignite Modification Date:
2025-12-26 @ 2:11 AM
NCT ID:
NCT05065905
Group ID:
EG000
Title:
Interferon
Description:
All participants receive subcutaneous interferon-gamma (Ingaron®) 500,000 IU alternated with Interal® (interferon alpha) 3,000,000 IU every other day
Interventions:
Drug: Ingaron® Drug: Interal® Drug: Antituberculosis complex therapy
Interferon-Gamma: received by microbiological synthesis; specific antiviral activity on cells is 2x10\*7 Units per mg of protein
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
30
Other Number Affected:
0
Other Number At Risk:
30
Study:
NCT05065905
Results Section:
NCT05065905
Adverse Events Module:
NCT05065905