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 @ 11:53 AM
Ignite Modification Date:
2025-12-25 @ 11:54 AM
NCT ID:
NCT02501161
Group ID:
EG000
Title:
Insulin Degludec/Liraglutide
Description:
Participants received s.c. injection of IDegLira once daily up to 104 weeks. Participants received 10 dose steps (10 units IDeg/0.36 mg liraglutide) initially. The dose was then escalated twice weekly until the FPG target between 4.0-5.0 mmol/L (72-90 mg/dL) was reached. The maximum dose was 50 dose steps (50 units IDeg/1.8 mg liraglutide).
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
60
Serious Number At Risk:
506
Other Number Affected:
206
Other Number At Risk:
506
Study:
NCT02501161
Results Section:
NCT02501161
Adverse Events Module:
NCT02501161