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 |
|---|---|---|---|---|---|---|---|---|
| Jetstream Atherectomy System | Patients with symptomatic peripheral vascular disease undergoing percutaneous intervention including Atherectomy utilizing the Jetstream Atherectomy System with or without adjunctive therapy. Jetstream Atherectomy System: Atherectomy | None | None | 42 | 241 | 38 | 241 | View |
Serious Events
| Term | Type | Organ System | Vocab | View |
|---|---|---|---|---|
| Target Vessel Revascularization/ Target Lesion Revascularization | SYSTEMATIC_ASSESSMENT | Vascular disorders | None | View |
| Distal Embolization Requiring a Separate Intervention | SYSTEMATIC_ASSESSMENT | Vascular disorders | None | View |
| Amputation | SYSTEMATIC_ASSESSMENT | Surgical and medical procedures | None | View |
Other Events
| Term | Type | Organ System | Vocab | View |
|---|---|---|---|---|
| Peripheral Artery Disease | SYSTEMATIC_ASSESSMENT | Vascular disorders | None | View |