Adverse Events Module
For researchers submitting trial data to ClinicalTrials.gov, the Adverse Events module is one of four mandatory results sections. It requires reporting in three primary categories: All-Cause Mortality: A table tracking all deaths that occurred during the study, regardless of cause. Serious Adverse Events (SAEs): A tabular summary of events resulting in death, life-threatening conditions, hospitalization, or significant disability. Other Adverse Events: A table for non-serious events that exceed a specific frequency threshold, such as 5% within any study arm.
Adverse Events Module path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Groups
Study -> Results Section -> Adverse Events Module -> Serious Events
Study -> Results Section -> Adverse Events Module -> Other Events
Adverse Events Module
Event Groups
| Title | Description | Deaths # Affected | Deaths # At Risk | Serious # Affected | Serious # At Risk | Other # Affected | Other # At Risk | View |
|---|---|---|---|---|---|---|---|---|
| Control | Schools which receive no intervention | 0 | None | 0 | 1629 | 0 | 1629 | View |
| PATHS to PAX | Universal classroom-based preventive intervention designed to reduce aggression. PATHS to PAX: A universal classroom-based preventive intervention designed to prevent aggression. | 0 | None | 0 | 1792 | 0 | 1792 | View |
| PATHS to PAX and the IncredibleYears | The combination of PATHS to PAX with the Incredible Years child and parent groups. PATHS to PAX and the Incredible Years: A universal classroom-based preventive intervention in combination with an indicated preventive intervention, both of which are designed to prevent aggression. | 0 | None | 0 | 1812 | 0 | 1812 | View |