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 |
|---|---|---|---|---|---|---|---|---|
| Exparel | This arm will receive intraoperative local Liposomal Bupivacaine injection (Exparel) at the port placement site. Exparel: This group will receive intraoperative local Liposomal Bupivacaine injection at the surgical site. | 0 | None | 6 | 63 | 0 | 63 | View |
| Marcaine | This group will receive will local bupivacaine HCl (Marcaine) injection at the port placement site. Marcaine: This group will receive intraoperative Bupivacaine HCl injection at the surgical site. | 0 | None | 6 | 73 | 0 | 73 | View |
Serious Events
| Term | Type | Organ System | Vocab | View |
|---|---|---|---|---|
| Postoperative Ileus | NON_SYSTEMATIC_ASSESSMENT | Gastrointestinal disorders | None | View |
| Postoperative Bleeding | NON_SYSTEMATIC_ASSESSMENT | Surgical and medical procedures | None | View |
| Postoperative Hypotension | NON_SYSTEMATIC_ASSESSMENT | Surgical and medical procedures | None | View |
| Stricture | NON_SYSTEMATIC_ASSESSMENT | Renal and urinary disorders | None | View |