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 @ 11:55 PM
Ignite Modification Date: 2025-12-25 @ 9:51 PM
NCT ID: NCT02951351
Description: None
Frequency Threshold: 0
Time Frame: Study treatment follow up was defined as one year following last administration of study treatment.
Study: NCT02951351
Study Brief: Topical Proparacaine Eye Drops to Improve the Experience of Patients Undergoing Intravitreal Injections
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Standard Procedure + Culture Patients will undergo the standard injection protocol. A conjunctival culture will then be obtained followed by the application of povidone-iodine to the eyelashes and eyelid margins. Patients will be randomized to receive 5% povidone-iodine drop to the conjunctival surface followed by conjunctival culture then re-application of 5% povidone-iodine drop to the conjunctival surface. Injection will then proceed. Conjunctival culture: Conjunctival cultures will be performed to ensure that the intervention does not interfere with antisepsis. 0 None 0 19 0 19 View
Proparacaine + Culture Patients will undergo the standard injection protocol. A conjunctival culture will then be obtained followed by the application of povidone-iodine to the eyelashes and eyelid margins. Patients will undergo application of another drop of topical anesthetic followed by conjunctival culture. After the culture, this group of patients will have 5% povidone iodine applied to the conjunctival surface. Intravitreal injection will then proceed. Proparacaine: Extra proparacaine will be applied to the conjunctival surface to determine its role in patient experience. Conjunctival culture: Conjunctival cultures will be performed to ensure that the intervention does not interfere with antisepsis. 0 None 0 17 0 17 View
Serious Events(If Any):
Other Events(If Any):