Price Vision Group
Indianapolis, Indiana, 46260, United States
Location status: Recruiting
Location contact
Francis Price, MD
PRINCIPAL_INVESTIGATOR
Marianne Price, Ph.D
CONTACT
NCT Number: NCT03922542
The study objective is to compare accelerated and standard corneal crosslinking for treatment of progressive keratoconus or corneal ectasia.
Interested in participating?
Request Info10 year and older
All sexes
Interventional
Phase 2 / Phase 3
Indianapolis, Indiana, 46260, United States
Location status: Recruiting
Francis Price, MD
PRINCIPAL_INVESTIGATOR
Marianne Price, Ph.D
CONTACT
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
Contact information is provided by the study sponsor or research team.
Price Vision Group
Industry
Randomized Comparison of Standard vs. Accelerated Corneal Crosslinking for Treatment of Progressive Keratoconus or Ectasia
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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