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 |
|---|---|---|---|---|---|---|---|---|
| Conventional Microscope (Re-randomized) | Participants who had a procedure for their second eye were re-randomized to use of a conventional microscope for the procedure. | 0 | None | 0 | 1 | 0 | 1 | View |
| Conventional Microscope | Participants randomized to the use of a conventional microscope for the first eye procedure. Participants who had a procedure for their second eye were randomized again to either the conventional or NGENUITY microscope. | 0 | None | 0 | 14 | 0 | 14 | View |
| NGENUITY | Participants randomized to the use of a NGENUITY microscope for the first eye procedure. Participants who had a procedure for their second eye were randomized again to either the conventional or NGENUITY microscope. | 0 | None | 0 | 14 | 0 | 14 | View |
| NGENUITY (Re-randomized) | Participants who had a procedure for their second eye were re-randomized to use of the NGENUITY microscope for the procedure. | 0 | None | 0 | 3 | 0 | 3 | View |