Other Event

Other Event

Other Adverse Events are non-serious adverse events that exceed a specific frequency threshold (typically 5% within any study arm). These events are reported to provide comprehensive safety information about all noteworthy adverse occurrences during clinical trials. Each other event is categorized by term, organ system, assessment type, and source vocabulary for standardized reporting.

Other Event path is as follows:

Study -> Results Section -> Adverse Events Module -> Other Event

Study -> Results Section -> Adverse Events Module -> Other Event -> Other Event Stats

Other Event


Ignite Creation Date: 2025-12-24 @ 11:37 PM
Ignite Modification Date: 2025-12-25 @ 9:27 PM
NCT ID: NCT02780856
Term: Device Deficiency
Organ System: Product Issues
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: ISO 14155:2011(E)
Notes: Device Deficiency - inadequacy of a medical device with respect to its identity, quality, durability, reliability, safety or performance
Study: NCT02780856
Study Brief: Safety and Performance Evaluation of the Calcivis System
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG000 3 3 110 View