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 @ 4:06 AM
Ignite Modification Date:
2025-12-26 @ 3:02 AM
NCT ID:
NCT02972502
Group ID:
EG000
Title:
Metoclopramide (Reglan)
Description:
Patients will receive 10 mg of intravenous (IV) metoclopramide following a 1-liter bolus of normal saline (NS) and 25 mg of IV diphenhydramine.
Metoclopramide: Patients receive 10 mg of intravenous (IV) metoclopramide.
Normal Saline: All patients receive a 1-liter bolus of normal saline (NS)
Diphenhydramine: All patients receive 25 mg of intravenous (IV) diphenhydramine.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
26
Other Number Affected:
0
Other Number At Risk:
26
Study:
NCT02972502
Results Section:
NCT02972502
Adverse Events Module:
NCT02972502