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 @ 12:05 AM
Ignite Modification Date:
2025-12-25 @ 10:03 PM
NCT ID:
NCT02260258
Group ID:
EG000
Title:
Rocuronium
Description:
Patients will receive a bolus dose of 1 mg/kg, then a continuous I.V. infusion as per standard intensive care unit practice.
Of note, protocol allows for use of cistatracurium in place of rocuronium for either reasons of drug-shortage or clinical conditions (if institutional preferences for dose adjustment in liver or renal insufficiency arise).
Rocuronium: Neuromuscular Blockade
Deaths Number Affected:
23
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
37
Other Number Affected:
0
Other Number At Risk:
37
Study:
NCT02260258
Results Section:
NCT02260258
Adverse Events Module:
NCT02260258