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 @ 9:25 PM
Ignite Modification Date:
2025-12-25 @ 7:10 PM
NCT ID:
NCT00908232
Group ID:
EG000
Title:
Complete to Partial Response: Bortezomib + Dexamethasone
Description:
Complete, very good partial or partial response after 4 cycles bortezomib + dexamethasone: bortezomib 1.3 mg/m2 IV bolus on Day 1, 4, 8, 11 in combination with dexamethasone 20 mg orally daily, on Days 1, 2, 4, 5, 8, 9, 11, 12 for cycle 5 to 8
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
59
Serious Number At Risk:
144
Other Number Affected:
137
Other Number At Risk:
144
Study:
NCT00908232
Results Section:
NCT00908232
Adverse Events Module:
NCT00908232