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 |
|---|---|---|---|---|---|---|---|---|
| EZ Pass Suture Passer | Patients who have surgery using the EZ Pass Suture Passer Instrument either in rotator cuff or soft tissue repair EZ Pass Suture Passer: open or arthroscopic instrument utilized in conjunction with a nitinol wire or nylon monofilament to aid in passing suture through soft tissue | 0 | None | 0 | 51 | 5 | 51 | View |
| Precision Flexible Reamer | Patients who have surgery using the Precision Flexible Reamer Instrument in ACL repair Precision Flexible Reamer: handheld device intended to be used in ACL and PCL reconstruction surgeries to manipulate tissue, or in conjunction with other devices in these surgeries. | 0 | None | 0 | 22 | 2 | 22 | View |