Accelerated Corneal Collagen Crosslinking for Keratoconus and Ectasia Using Pulse or Continuous UV-A Light

Keratoconus Clinical Trial

Official title:

A Randomized Study to Evaluate the Safety and Efficacy of Corneal Collagen Crosslinking Performed With Continuous vs Pulsed UVA Light for Reducing Corneal Curvature in Eyes With Keratoconus and Post-refractive Corneal Ectasia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05027295
• Other study ID #: ACCEL-CXL-001
• Status: Recruiting
• Phase: Phase 3
• Start date: July 30, 2021
• Est. completion date: July 2025

Study information

• Verified date: December 2022
• Source: Cornea and Laser Eye Institute
• Contact: BethAnn Furlong-Hibbert
• Phone: (201) 692-9434
• Email: bfurlong-hibbert[@]vision-institute.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Corneal collagen crosslinking has been demonstrated as an effective method of reducing progression of both keratoconus and post-refractive corneal ectasia, as well as decreasing the steepness of the cornea in these pathologies.

Performing an accelerated CXL procedure with pulsed UVA light may increase the oxygenation of the cornea, which may improve the crosslinking efficacy.

Description:

This is a prospective, single-site study to analyze the use of continuous vs pulsed UVA light after removal of the epithelium for the collagen crosslinking procedure for keratoconus and post-refractive corneal ectasia. In the standard crosslinking treatment, the cornea is treated with a continuous UVA light treatment with a power of 3mW/cm2 for 30 minutes. CXL treatment can potentially be performed in a shorter period of time by increasing the power of the UVA light and decreasing the exposure time, while maintaining the same total energy delivered to the cornea. This study will compare the efficacy and safety of accelerated crosslinking using either a continuous or pulsed UVA treatment. One group will be randomized to be treated with 12mW/cm2 of continuous UVA light treatment for 7.5 minutes and the other group will be treated with 12mW/cm2 of pulsed UVA light treatment for 15 minutes.

The primary efficacy parameter that will be evaluated over time is maximum keratometry (Kmax) in the randomized eyes for each treatment group. The secondary efficacy parameter is to determine if the two treatment groups are equivalent in their mean Kmax change at 6 months after treatment compared with baseline.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 170
• Est. completion date: July 2025
• Est. primary completion date: July 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years of age or older having a diagnosis of keratoconus or corneal ectasia after corneal refractive surgery

• Presence of central or inferior corneal steepening on the Pentacam map

• Axial topography consistent with keratoconus or post-surgical corneal ectasia

• Contact lens wearers only: removal of contact lenses for the required period of 1 week prior to the screening refraction

• Signed written informed consent

• Willingness and ability to comply with schedule for follow-up visits

Exclusion Criteria:

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

• Corneal pachymetry measuring 300 microns or less 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, for example:

1. History of corneal disease (e.g. herpes simplex, herpes zoster keratitis, recurrent corneal erosion syndrome, corneal melt, corneal dystrophy, etc.

2. Clinically significant scarring in the CXL treatment zone

• A history of chemical injury or delayed healing in the eye(s) to be treated

• 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 current condition that, in the investigator's opinion, would interfere with or prolong epithelial healing

Related Conditions & MeSH terms

• Corneal Diseases
• Corneal Ectasia
• Keratoconus

Intervention

Drug:
• riboflavin ophthalmic solution
Administration of riboflavin one drop every 2 minutes during administration of continuous UVA light for 7.5 minutes.
• riboflavin ophthalmic solution
Administration of riboflavin one drop every 2 minutes during administration of pulsed UVA light for 15 minutes

Locations

Country	Name	City	State
United States	Cornea and Laser Eye Institute, Hersh Vision Group	Teaneck	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
Cornea and Laser Eye Institute

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum keratometry	The change in maximum keratometry (Kmax) from baseline will be evaluated at 6 months	6 months
Secondary	Mean keratometry	Determine whether the two treatment groups are equivalent in their mean keratometry (meanK) change at 6 months post treatment compared with baseline.	6 months