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 |
|---|---|---|---|---|---|---|---|---|
| Group 1: Extended Release Tolterodine | 4 mg Tolterodine po daily for 12-weeks At 12 Weeks, the subjects were offered the addition of the alternative therapy with follow-up at 24 and 52 weeks. | 0 | None | 0 | 30 | 17 | 30 | View |
| Group 2: Intra Vaginal Estradiol Cream | 0.5 grams of Intra vaginal estradiol cream nightly for 6 weeks, then twice weekly for 6 weeks At 12 Weeks, the subjects were offered the addition of the alternative therapy with follow-up at 24 and 52 weeks. | 0 | None | 0 | 28 | 6 | 28 | View |