Bandage Contact Lenses for Corneal Abrasions

Corneal Abrasion Clinical Trial

Official title: Bandage Contact Lenses to Decrease Pain and Improve Healing in Emergency Department Subjects Presenting With Corneal Abrasions

Status Recruiting

Clinical Trial Summary

Two percent of all patients presenting to the Emergency Departments have complaints involving the eye. Corneal abrasions are a common diagnosis with patients with eye pain and often cause significant discomfort. Current treatment includes a thorough evaluation of the eye followed by patching, empiric antibiotics, cycloplegics and oral pain medicines. This study will be a randomized controlled trial to determine the safety and efficacy of BCLs. It will involve the initial patient evaluation followed by a return visit to the Emergency Department within 36 hours for re-examination. At each visit, the patient will be assessed for the size and location of the abrasion along with their report of pain using a visual analog scale. Data will be recorded on a standard data collection sheet. Telephone contact will be made at 30 days to ensure resolution of abrasion and that no complications ensued.

Clinical Trial Description

n/a

Related Conditions & MeSH terms

• Corneal Abrasion
• Eye Injuries
• Eye Trauma

• NCT number: NCT03206723
• Study type: Interventional
• Source: Los Angeles Biomedical Research Institute
• Contact: David Tanen, MD
• Phone: 3102223501
• Email: dtanen@labiomed.org
• Status: Recruiting
• Phase: Phase 2
• Start date: July 1, 2017
• Completion date: March 1, 2019