Standard versus transepithelial corneal crosslinking for treatment of progressive keratoconus

Completed

• Conditions: corneal deformation; Keratoconus; 10015920; 10042261

• Registration Number: NL-OMON39491
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 62

Inclusion Criteria

Patient age of >= 18 years, documented progressive KC (by Pentacam and/or corneal topography imaging), a clear central cornea, minimal corneal thickness of at the thinnest corneal location (Pentacam imaging), minimal Snellen corrected distance visual acuity of >= 0.4.

Exclusion Criteria

Patient age less than 18 years, stable keratometry values over time, presence of corneal scar(s)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The main study parameter is the keratometry outcome over a period of 1 year,<br /><br>which is measured by corneal topography and Pentacam imaging. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>The secondary objective is the incidence of epithelial healing problems after<br /><br>treatment.</p><br>