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 @ 1:10 PM
Ignite Modification Date:
2025-12-25 @ 12:22 PM
NCT ID:
NCT00513461
Group ID:
EG000
Title:
Arm I (SAMe)
Description:
Patients receive SAMe PO QD for weeks 1-4, PO BID for weeks 5-8, and PO TID for weeks 9-24 in the absence of disease progression or unacceptable toxicity.
S-adenosyl-L-methionine disulfate p-toluene-sulfonate: Given PO
laboratory biomarker analysis: Correlative studies
immunoenzyme technique: Correlative studies
high performance liquid chromatography: Correlative studies
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
57
Other Number Affected:
51
Other Number At Risk:
57
Study:
NCT00513461
Results Section:
NCT00513461
Adverse Events Module:
NCT00513461