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 @ 9:13 PM
Ignite Modification Date:
2025-12-25 @ 7:03 PM
NCT ID:
NCT00104104
Group ID:
EG001
Title:
30 - Minute Infusion
Description:
Participants received 4 mg zoledronic acid intravenously, in 250 mL of fluid, every 3-4 weeks for up to 24 months, over a 30-minute infusion time, but increasing to a 45-minute infusion time if they experienced a clinically relevant rise in serum creatinine that resolved in less than 12-weeks.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
84
Other Number Affected:
76
Other Number At Risk:
84
Study:
NCT00104104
Results Section:
NCT00104104
Adverse Events Module:
NCT00104104