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
| Title | Description | Deaths # Affected | Deaths # At Risk | Serious # Affected | Serious # At Risk | Other # Affected | Other # At Risk | View |
|---|---|---|---|---|---|---|---|---|
| Type 2 Diabetes - GL Then NGL | Participants with Type 2 Diabetes received Glycogen loading (GL) followed by Non-Glycogen loading (NGL) meal after 3-6 weeks of washout | 0 | None | 0 | 6 | 0 | 6 | View |
| Type 2 Diabetes - NGL Then GL | Participants with Type 2 Diabetes received Non-Glycogen loading (NGL) followed by Glycogen loading (GL) meal after 3-6 weeks of washout | 0 | None | 0 | 8 | 0 | 8 | View |
| Participants Without Diabetes - GL Then NGL | Participants with no Diabetes received Glycogen loading (GL) followed by Non-Glycogen loading (NGL) meal after 3-6 weeks of washout | 0 | None | 0 | 7 | 0 | 7 | View |
| Participants Without Diabetes - NGL Then GL | Participants with Type 2 Diabetes received Non-Glycogen loading (NGL) followed by Glycogen loading (GL) meal after 3-6 weeks of washout | 0 | None | 0 | 8 | 0 | 8 | View |