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 @ 11:18 PM
Ignite Modification Date:
2025-12-25 @ 8:57 PM
NCT ID:
NCT04104256
Group ID:
EG000
Title:
Alert 1
Description:
Patients with a pre-op encounter in which the physician attempts to place an order for a pre-op test. Physician has been assigned to the Nudge #1 group
Nudge #1: Alert highlighting the safety/potential harms to patients of undergoing pre-op tests: Nudge 1:
* UCLA Ophthalmologists and Anesthesiologists ADVISE AGAINST routine pre-op testing.
* UCLA Pre-op Eval and Planning Center (PEPC) will order any needed labs on the day of surgery.
* Routine pre-op tests are inappropriate.
* Routine pre-op tests do NOT increase patient safety and go AGAINST local and national guidelines Hard stop before allowing the ordering of a pre-op test where physicians must provide accountable justification: "EXPLAIN WHY GOING AGAINST GUIDELINES"
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
269
Other Number Affected:
9
Other Number At Risk:
269
Study:
NCT04104256
Results Section:
NCT04104256
Adverse Events Module:
NCT04104256