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 @ 10:23 PM
Ignite Modification Date:
2025-12-25 @ 7:55 PM
NCT ID:
NCT05064735
Group ID:
EG000
Title:
Semaglutide 2.4 mg
Description:
Participants initiated at a once-weekly dose of 0.24 mg semaglutide s.c. as a adjunct to a reduced calorie diet and increased physical activity and followed a fixed-dose escalation regimen, with dose increase every 4 weeks (to doses of 0.5, 1.0, 1.7 and 2.4 mg/week), until the target dose was reached after 16 weeks. Participants continued 2.4 mg semaglutide s.c. once- weekly from week 16 to week 68 as a adjunct to a reduced calorie diet and increased physical activity. Participants were followed up for 7 weeks after end of treatment till week 75.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
27
Serious Number At Risk:
269
Other Number Affected:
128
Other Number At Risk:
269
Study:
NCT05064735
Results Section:
NCT05064735
Adverse Events Module:
NCT05064735