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:
EG000
Title:
Open Label (OL) (PEG-IFN, RBV); OL Randomized (PEG-IFN)
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 receive the pegylated interferon (PEG-IFN) 180 mcg weekly Arm.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
44
Other Number Affected:
43
Other Number At Risk:
44
Study:
NCT00078403
Results Section:
NCT00078403
Adverse Events Module:
NCT00078403