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 @ 4:07 AM
Ignite Modification Date:
2025-12-26 @ 3:04 AM
NCT ID:
NCT00946920
Group ID:
EG000
Title:
Degarelix 240 mg/480 mg
Description:
Degarelix: The degarelix doses were administered by subcutaneous (s.c.) injections into the abdominal wall. A starting dose of 240 mg degarelix was administered on Day 0. One month later a maintenance dose of 480 mg was administered. This was repeated after 4, 7, and 10 months (ie a total of 5 administrations).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
58
Serious Number At Risk:
565
Other Number Affected:
336
Other Number At Risk:
565
Study:
NCT00946920
Results Section:
NCT00946920
Adverse Events Module:
NCT00946920