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Clinical Trial Summary

The objective of this study was to show that patients with corneal abrasions would experience more pain relief with short term topical tetracaine than placebo, have similar complication rates, and take less hydrocodone for breakthrough pain.


Clinical Trial Description

Corneal abrasions are among the most common eye-related injuries seen in the emergency department (ED). Topical anesthetic drops are routinely used prior to slit-lamp examination for diagnosis of corneal abrasions and often provide immediate pain relief. Patients are then sent home with oral analgesics and topical antibiotics. The use of topical anesthetics for outpatient treatment of corneal abrasions is discouraged by most emergency medicine textbooks due to concerns over safety. Case reports of abuse and misuse as well as animal studies have suggested that long term use of topical anesthetics may lead to rare complications. Two clinical trials showed no delayed healing after a short course of topical anesthetics following PRK surgery. Whether this could be applied to nonsurgical patients in the ED was investigated by two small clinical trials that showed similar efficacy and safety but were underpowered to prove a statistical difference. In 2014, a larger randomized trial demonstrated the safety of tetracaine for ED patients with corneal abrasions but failed to show a significant difference in patient visual analogue scale (VAS) pain ratings over time. More recently, a retrospective cohort study of 444 ED patients given tetracaine for 24 hours reported no serious complications or uncommon adverse events. If topical anesthetics could be safely prescribed for short term use in the management of corneal abrasions, it is possible that this would decrease use of systemic opioids for this purpose. The aim of this randomized, double-blind trial was to compare the effectiveness of topical tetracaine versus placebo in ED patients with corneal abrasions as measured by a reduction in the VAS score. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04187417
Study type Interventional
Source INTEGRIS Southwest Medical Center
Contact
Status Completed
Phase N/A
Start date January 1, 2015
Completion date September 30, 2018

See also
  Status Clinical Trial Phase
Terminated NCT04159714 - Bandage Contact Lens Application for the Management of Corneal Abrasion N/A
Withdrawn NCT02483897 - Effect of Tetracaine on Pain Management and Corneal Healing in Patients With Acute Corneal Abrasion Phase 3
Recruiting NCT03206723 - Bandage Contact Lenses for Corneal Abrasions Phase 2
Not yet recruiting NCT05534217 - The Debridement To Treat The Traumatic Corneal Abrasion N/A