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 @ 9:18 PM
Ignite Modification Date:
2025-12-25 @ 7:06 PM
NCT ID:
NCT01422304
Group ID:
EG001
Title:
Usual Care
Description:
For participants in this Arm assigned to planned active reversal of neuromuscular blockade: single IV administration of neostigmine (up to a maximum dose of 5 mg) with glycopyrrolate or atropine and single IV administration of placebo (normal saline \[NaCl 0.9%\] to match volume of sugammadex that would have been administered). For participants in this Arm assigned to planned spontaneous recovery from neuromuscular blockade: single IV administration of placebo (normal saline \[NaCl 0.9%\] to match volume of sugammadex that would have been administered).
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
40
Serious Number At Risk:
588
Other Number Affected:
499
Other Number At Risk:
588
Study:
NCT01422304
Results Section:
NCT01422304
Adverse Events Module:
NCT01422304