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:
2025-12-25 @ 3:20 AM
Ignite Modification Date:
2025-12-26 @ 1:58 AM
NCT ID:
NCT00454805
Group ID:
EG001
Title:
Placebo
Description:
Placebo+Fulvestrant 250 mg
Patients randomised to the control arm (fulvestrant + placebo) received treatment according to the following schedule:
* Day 1: fulvestrant 500 mg im
* Day 15: fulvestrant 250 mg im
* Day 29, and every 28 days thereafter: fulvestrant 250 mg im
* and daily: placebo to match cediranib (administered orally)
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
31
Other Number Affected:
30
Other Number At Risk:
31
Study:
NCT00454805
Results Section:
NCT00454805
Adverse Events Module:
NCT00454805