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 @ 9:47 PM
Ignite Modification Date: 2025-12-25 @ 7:26 PM
NCT ID: NCT04045132
Term: Protocol Deviation- Unstamped Version of Informed Consent
Organ System: Psychiatric disorders
Assessment Type: NON_SYSTEMATIC_ASSESSMENT
Source Vocabulary: None
Notes: A minor protocol deviation occurred and a version of the informed consent was used that was not stamped by the IRB. The content of the unstamped ICF was identical to the IRB stamped version, the physical forms were just missing the IRB approval stamp
Study: NCT04045132
Study Brief: Social Media-Based Parenting Program for Women With Postpartum Depressive Symptoms
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG001 6 6 38 View
EG000 6 6 37 View