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 @ 12:54 PM
Ignite Modification Date:
2025-12-25 @ 12:18 PM
NCT ID:
NCT01585961
Group ID:
EG000
Title:
Catheter Ablation
Description:
These patients have drug refractory, recurrent, symptomatic paroxysmal atrial fibrillation, are aged 18 years or older, and are able and willing to provide written informed consent to participate in the study.
Catheter Ablation (NAVISTAR® THERMOCOOL® SF Catheter): Administer anesthesia according to standard EP lab protocol, assess the fluid status of the subject (after each liter of infusate), determine if diuresis is necessary, and treat accordingly.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
63
Serious Number At Risk:
508
Other Number Affected:
79
Other Number At Risk:
508
Study:
NCT01585961
Results Section:
NCT01585961
Adverse Events Module:
NCT01585961