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 @ 9:46 PM
Ignite Modification Date: 2025-12-25 @ 7:26 PM
NCT ID: NCT05320432
Description: None
Frequency Threshold: 0
Time Frame: 2 weeks post-procedure
Study: NCT05320432
Study Brief: Transcutaneous Electrical Nerve Stimulation for Pain Control During First-trimester Abortion
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Transcutaneous Electrical Nerve Stimulation (TENS) Prior to the procedure, the patient will have two sets of two self-adhesive electrodes placed parallel to the spinal cord at the T10-L1 and S2-S4 levels for TENS administration. For participants randomized to the experimental group, the non-blinded study coordinator will turn on the TENS unit 5 minutes prior to the procedure and monitor stimulating frequency level (80-100 Hz and pulse duration of 400 microseconds; intensity or frequency will be monitored to be administered to a non-painful level). Transcutaneous electrical nerve stimulation (TENS): A low-level electrical current through the skin activates the descending inhibitory systems in the central nervous system. 0 None 0 35 0 35 View
Sham For the participants randomized to sham, the same placement of electrodes will occur, but the unit will not be delivering electrical stimulation. Sham: No current applied through pads. 0 None 0 35 0 35 View
Serious Events(If Any):
Other Events(If Any):