Price Vision Group
Indianapolis, Indiana, 46260, United States
NCT Number: NCT03922542
The study objective is to compare accelerated and standard corneal crosslinking for treatment of progressive keratoconus or corneal ectasia.
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Notify Me10 year and older
All sexes
Interventional
Phase 2 / Phase 3
Indianapolis, Indiana, 46260, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Use of riboflavin 0.1% eye drops and 9 mW/cm2 UVA light for 10 minutes
Time frame: 6 months
assessed by corneal tomography
Time frame: 6 months
assessed with Snellen chart
Time frame: 6 months
assessed with Snellen chart
Price Vision Group
Industry
Randomized Comparison of Standard vs. Accelerated Corneal Crosslinking for Treatment of Progressive Keratoconus or Ectasia
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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