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 @ 7:50 PM
Ignite Modification Date:
2025-12-25 @ 5:26 PM
NCT ID:
NCT05076604
Group ID:
EG001
Title:
Microplegia
Description:
Nondiluted microplegia consists of all parts human blood.
Microplegic Solution No. 1: The microplegia solution that is standard of care for all cardiac surgery patients, and which all study subjects will receive is:
Induction 240 mL Baxter Cardioplegia Solution 10. 5 mL Potassium Chloride 2 meq/ml (21 meq) 250.5 mL total volume
Maintenance 747 mL Baxter Cardioplegia Solution 3.4 mL Potassium Chloride 2 meq/ml (6.75 meq) 750.4 mL total volume
Subjects will be randomly assigned to 4:1 cardioplegia or nondiluted microplegia.
4:1 cardioplegia consists of 4 parts crystalloid intravenous fluid to one part human blood.
Nondiluted microplegia consists of all parts human blood.
Deaths Number Affected:
7
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
157
Other Number Affected:
56
Other Number At Risk:
157
Study:
NCT05076604
Results Section:
NCT05076604
Adverse Events Module:
NCT05076604