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 @ 7:11 PM
NCT ID:
NCT00887432
Group ID:
EG000
Title:
Cholecalciferol
Description:
Patients receive cholecalciferol PO QD for 9 months in the absence of disease progression or unacceptable toxicity.
Cholecalciferol: Given PO
Laboratory Biomarker Analysis: Correlative studies
Patient Observation
Placebo Administration: Given PO
Quality-of-Life Assessment: Ancillary studies
Questionnaire Administration: Ancillary studies
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
119
Other Number Affected:
2
Other Number At Risk:
119
Study:
NCT00887432
Results Section:
NCT00887432
Adverse Events Module:
NCT00887432