Adverse Events Module

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


Ignite Creation Date: 2025-12-24 @ 6:39 PM
Ignite Modification Date: 2025-12-25 @ 4:09 PM
NCT ID: NCT05613257
Description: None
Frequency Threshold: 0
Time Frame: Adverse event data was collected for the first 30 days after surgery.
Study: NCT05613257
Study Brief: Distal Targeter vs Free-hand
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Free-hand/Perfect Circles Patients in this group will have interlocking screw placement using a free-hand, perfect circles technique. Free-hand/perfect circles technique: Patients in this arm will have no assistive targeting device use and the surgeon will use a free-hand technique for the placement of interlocking screws. With this technique, fluoroscopic images are taken such that the interlocking holes of the intramedullary device are "perfect circles" and indicate that a screw introduced in the same plane that the fluoroscopic image was taken would seat perpendicularly to the intramedullary device. This is the most commonly employed technique for interlocking screw placement through intramedullary devices. 0 None 0 33 0 33 View
Distal Targeting Jig Patients in this group will have interlocking screw placement using a proximally placed distal targeting jig Distal targeting jig: Patients in this arm will have an assistive targeting device used for interlocking screw placement. The targeting device is attached to the nail proximally or distally (for antegrade or retrograde nailing, respectively) to guide screw placement through the other end of the intramedullary device. 0 None 0 29 0 29 View
Serious Events(If Any):
Other Events(If Any):