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 @ 11:49 PM
Ignite Modification Date:
2025-12-25 @ 9:43 PM
NCT ID:
NCT00363051
Group ID:
EG000
Title:
Stratum 1: Everolimus 10 mg
Description:
Stratum 1 patients who were not receiving regular Octreotide Depot therapy. These patients were to receive everolimus monotherapy at 10 mg/day. Patients were instructed to take two 5 mg tablets of everolimus orally with a glass of water, once daily (preferably in the morning). Dosing was strongly recommended to occur at the same time every day.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
63
Serious Number At Risk:
115
Other Number Affected:
115
Other Number At Risk:
115
Study:
NCT00363051
Results Section:
NCT00363051
Adverse Events Module:
NCT00363051