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 @ 10:35 PM
Ignite Modification Date:
2025-12-25 @ 8:06 PM
NCT ID:
NCT05067335
Group ID:
EG002
Title:
Placebo/Romosozumab
Description:
After completion of the 6-month Double-blind Period, participants initially randomized to placebo arm switched to receive romosozumab 210 mg sc QM during the 6-month Open-label (OL) Period (up to Month 12).
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
98
Other Number Affected:
59
Other Number At Risk:
98
Study:
NCT05067335
Results Section:
NCT05067335
Adverse Events Module:
NCT05067335