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 |
|---|---|---|---|---|---|---|---|---|
| Group A | Full dose, pre-hospital fibrinolysis followed by treatment in the coronary care unit | None | None | 0 | 37 | 0 | 37 | View |
| Group B | One-half dose pre-hospital reteplase followed by urgent PCI | None | None | 9 | 253 | 0 | 253 | View |
| Group C | Fibrinolytic ineligible patients, treated with primary PCI at the STEMI center | None | None | 4 | 37 | 0 | 37 | View |
| Group D | Patients not transported by participating EMS units but were transferred in and treated with primary PCI at the STEMI center | None | None | 0 | 63 | 0 | 63 | View |
Serious Events
| Term | Type | Organ System | Vocab | View |
|---|---|---|---|---|
| Death | SYSTEMATIC_ASSESSMENT | Cardiac disorders | None | View |