Clinical Trials Directory

Trials / Recruiting

RecruitingNCT03922542

Comparison of Standard vs. Accelerated Corneal Crosslinking

Randomized Comparison of Standard vs. Accelerated Corneal Crosslinking for Treatment of Progressive Keratoconus or Ectasia

Status
Recruiting
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
510 (estimated)
Sponsor
Price Vision Group · Industry
Sex
All
Age
10 Years
Healthy volunteers
Not accepted

Summary

The study objective is to compare accelerated and standard corneal crosslinking for treatment of progressive keratoconus or corneal ectasia.

Conditions

Interventions

TypeNameDescription
COMBINATION_PRODUCTriboflavin 0.1%Use of riboflavin 0.1% eye drops and 9 mW/cm2 UVA light for 10 minutes
COMBINATION_PRODUCTRiboflavin 0.1%Use of riboflavin 0.1% eye drops and 3 mW/cm2 UVA light for 30 minutes

Timeline

Start date
2019-04-16
Primary completion
2026-06-01
Completion
2026-07-01
First posted
2019-04-22
Last updated
2025-07-31

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03922542. Inclusion in this directory is not an endorsement.