NCT Number: NCT01739673
Ultraviolet-A and Riboflavin Treatment for Infectious Keratitis
This study is to evaluate the efficacy of ultraviolet-A (UVA) and riboflavin application (also often referred to as corneal collagen crosslinking) as a method to enhance treatment of infectious keratitis.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Schwartz Laser Eye Center, Scottsdale, Arizona, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subjects must be 18 years of age or older.
- Ability to provide written informed consent.
- Likely to complete all study visits.
- Subjects must have one eye that with a diagnosis of infectious keratitis.
Exclusion criteria
- A corneal perforation.
- Descemetocele.
- Pregnancy or breastfeeding.
- Active Herpes corneal disease.
- Patient is unwilling or unable to comply with a medication regimen and follow up appointments.
Treatment and study plan
Primary outcomes
-
Resolution of Signs and Symptoms of Infectious Keratitis
Time frame: Subjects will be followed until resolution of signs and symptoms, an expected average of 8 weeks
Sponsors and collaborators
Lead sponsor
Cxlusa
Industry
Registry information
Important dates
- Study start
- 2011
- Primary completion
- 2014
- Study completion
- 2014
- First posted
- Dec 3, 2012
- Registry last updated
- Sep 26, 2018
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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