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 |
|---|---|---|---|---|---|---|---|---|
| Soymilk Consumption | Participants consumed 460 mL of soymilk in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |
| Placebo for Soymilk Consumption | Participants consumed 460 mL of 2% reduced fat milk in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |
| Green Tea Consumption | Participants consumed 460 ml of green tea made from 2 servings (4 g) in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |
| Placebo for Green Tea Consumption | Participants consumed 460 ml of water in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |
| Blueberry Consumption | Participants consumed 460 ml of blueberry powder (50 g) in water in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |
| Placebo for Blueberry Consumption | Participants consumed 460 ml of blueberry powder placebo (50 g) in water in a single dose. | 0 | None | 0 | 16 | 0 | 16 | View |