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 @ 12:56 PM
Ignite Modification Date:
2025-12-25 @ 12:18 PM
NCT ID:
NCT00048061
Group ID:
EG001
Title:
Ibandronate 50/50 mg
Description:
Participants received 100 mg ibandronate PO monthly taken on a single day (2 X 50 mg tablets) and round placebo tablet PO daily. Participants also received calcium 500 mg /day and vitamin D 400 IU/day.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
54
Serious Number At Risk:
396
Other Number Affected:
190
Other Number At Risk:
396
Study:
NCT00048061
Results Section:
NCT00048061
Adverse Events Module:
NCT00048061