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 @ 7:46 PM
Ignite Modification Date:
2025-12-25 @ 5:23 PM
NCT ID:
NCT00078403
Group ID:
EG001
Title:
OL (PEG-IFN, RBV) Then OL Randomized (Observation)
Description:
At week 12 (end of the initial run-in period - Step 1) participants were found to be HCV RNA positive (HCV RNA \> 60 IU/mL) and had less than a 2 log decrease in HCV RNA from Baseline. For Step 2, participants were assigned to the Randomized Open Label (OL) part of the study to be followed on the Observation (no treatment) Arm.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
42
Other Number Affected:
41
Other Number At Risk:
42
Study:
NCT00078403
Results Section:
NCT00078403
Adverse Events Module:
NCT00078403