Comparison of Standard vs. Accelerated Corneal Crosslinking
Recruiting now · Phase 2/Phase 3
Conditions studied: Keratoconus, Ectasia Corneal
In brief
The study objective is to compare accelerated and standard corneal crosslinking for treatment of progressive keratoconus or corneal ectasia.
Key facts
- Study ID
- NCT03922542
- Run by
- Price Vision Group
- People needed
- 510
- Starts
- 2019-04-16
- Expected to finish
- 2026-07-01
- Last updated by the study team
- 2025-07-31
Who can join
Age: 10 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Documented keratoconus or ectasia after refractive surgery
You may not qualify if…
- Insufficient corneal thickness
- Ocular condition that may predispose the eye to complications
- History of chemical injury or delayed epithelial healing
- Condition that would interfere with or prolong epithelial healing
- Known sensitivity to treatment medications
- Pregnancy
Where it is running
- Price Vision Group — Indianapolis, Indiana, United States (enrolling)
Full record on ClinicalTrials.gov
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