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 |
|---|---|---|---|---|---|---|---|---|
| Instructor-led Learning | This group will train their technical CPR-skills with supervision by a tutor (either general practitioner or medical student, all trained in CPR teaching) Instructor-led learning: Supervision by a tutor (either general practitioner or medical student, all trained in CPR teaching) | 0 | None | 0 | 122 | 0 | 122 | View |
| Self-learning | This group will Train alone without supervision and without communicating with the other participants. Self-learning: Training without supervision | 0 | None | 0 | 118 | 0 | 118 | View |