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 |
|---|---|---|---|---|---|---|---|---|
| Treatment Arm | Patients in the Treatment arm received Xagrotin in combination to the standard of care for Covid19. Xagrotin: A group of patients were treated with Xagrotin with or without standard of care, the control group received stadard of care | 2 | None | 1 | 483 | 113 | 483 | View |
| Control Arm | Patients in the Control arm received the standard of care for Covid19. | 10 | None | 10 | 178 | 15 | 178 | View |
Serious Events
| Term | Type | Organ System | Vocab | View |
|---|---|---|---|---|
| Xagrotin | NON_SYSTEMATIC_ASSESSMENT | Blood and lymphatic system disorders | None | View |