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 @ 5:19 AM
Ignite Modification Date:
2025-12-26 @ 4:26 AM
NCT ID:
NCT00571727
Group ID:
EG000
Title:
Mecasermin
Description:
Participants who were entered from previous studies continued to receive mecasermin 80 to 120 mcg/kg SC twice daily and naïve-to-treatment participants were administered mecasermin 60 to 80 mcg/kg SC twice daily for 1 to 2 weeks, and then increased to 120 mcg/kg as tolerated.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
18
Serious Number At Risk:
92
Other Number Affected:
73
Other Number At Risk:
92
Study:
NCT00571727
Results Section:
NCT00571727
Adverse Events Module:
NCT00571727