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 @ 2:32 PM
Ignite Modification Date:
2025-12-25 @ 1:04 PM
NCT ID:
NCT04588259
Group ID:
EG000
Title:
NovoRapid: Run-in period
Description:
Participants received subcutaneous injections of NovoRapid thrice daily + insulin degludec once daily with or without metformin for 8 weeks. Insulin degludec dose was adjusted weekly by the investigator based on the mean of three pre-breakfast SMPG values measured on the last two days prior to and on the day of contact. If one of the SMPG values were below target (less than 4.0 mmol/L or 71 mg/dL) then the insulin degludec dose was adjusted according to the titration guideline specified in the protocol.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
9
Serious Number At Risk:
331
Other Number Affected:
32
Other Number At Risk:
331
Study:
NCT04588259
Results Section:
NCT04588259
Adverse Events Module:
NCT04588259