Overview

Transepithelial Corneal Collagen Crosslinking for Keratoconus and Corneal Ectasia

Status:
Active, not recruiting
Trial end date:
2021-12-01
Target enrollment:
0
Participant gender:
All
Summary
Corneal collagen crosslinking (CXL) has been proposed as an effective method of reducing progression of both keratoconus and corneal ectasia after surgery, as well as possibly decreasing the steepness of the cornea in these pathologies. During previous studies of the CXL procedure, the surface epithelial cells have been removed. Transepithelial crosslinking in which the epithelium is not removed has been proposed to offer a number of advantages over traditional crosslinking including an increased safety profile by reducing the risk for infection as no epithelial barrier will be broken, faster visual recovery and improved patient comfort in the early postoperative healing period.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Cornea and Laser Eye Institute
Treatments:
Dextrans
Riboflavin
Criteria
Inclusion Criteria:

- 18 years of age or older

- A diagnosis of keratoconus or a diagnosis of corneal ectasia after corneal refractive
surgery

- Vision with contact lenses or glasses is worse than 20/20

- Corneal thickness greater than 375 microns at the thinnest point

Exclusion Criteria:

- Eyes classified as either normal, atypical normal, or keratoconus suspect on the
severity grading scheme.

- Corneal pachymetry ≤ 350 microns at the thinnest point measured by Pentacam in the
eye(s) to be treated.

- Previous ocular condition (other than refractive error) in the eye(s) to be treated
that may predispose the eye for future complications

- Clinically significant corneal scarring in the CXL treatment zone

- Pregnancy (including plan to become pregnant) or lactation during the course of the
study

- A known sensitivity to study medications

- Patients with nystagmus or any other condition that would prevent a steady gaze during
the CXL treatment or other diagnostic tests.

- Patients with a current condition that, in the investigator's opinion, would interfere
with or prolong epithelial healing.