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 @ 4:42 AM
Ignite Modification Date:
2025-12-26 @ 3:43 AM
NCT ID:
NCT00703118
Group ID:
EG004
Title:
T12(DS)/PR48 - OVERALL TREATMENT
Description:
4 weeks of Placebo followed by 12 weeks of 750 mg telaprevir q8hr in combination with 48 weeks of Peg-IFN-alfa-2a and RBV at standard doses - TE AES during the overall treatment phase
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
32
Serious Number At Risk:
264
Other Number Affected:
260
Other Number At Risk:
264
Study:
NCT00703118
Results Section:
NCT00703118
Adverse Events Module:
NCT00703118