Unstable Corneas
Conditions
Keywords
crosslinking, cornea, keratoconus, ectasia, irradiance, riboflavin
Brief summary
The purpose of this study is to evaluate the Safety and Efficacy of Corneal Cross Linking in a Continuous Beam versus Pulsed Treatments across epithelium on and epithelium off surfaces.
Interventions
DRUGEpithelium-On Riboflavin
Riboflavin 0.1% Phosphate Sodium solution with Benzalkonium Chloride Preservative
DRUGEpithelium-Off Riboflavin
Riboflavin 0.1% Phosphate Sodium solution
DEVICEUV Light - Continuous Beam
5 minutes of constant UV exposure to saturated cornea
DEVICEUV Pulsed Beam
5 minutes of UV exposure to saturated cornea, alternating 1 minute of treatment with 1 minute rest for a total time of 10 minutes
Sponsors
Crowd Health Research, LTD
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Keratoconus: * 12 years of age or older * Having a clinical diagnosis of progressive keratoconus consistent with: 1. An increase of ≥ 1.00 D in the steepest keratometry value 2. An increase of ≥ 1.00 D in astigmatism manifest refraction 3. A myopic shift (decrease in the spherical equivalent) of ≥ 0.50 D on subjective manifest refraction * Presence of central or inferior steepening on the topography map. * Axial topography consistent with keratoconus * Steepest keratometry (Kmax) value ≥ 47.00 D * Signed written informed consent * Willingness and ability to comply with schedule for follow-up visits * Contact lens removal prior to evaluation and treatment Inclusion Criteria Post-Surgical Ectasia: * History of having undergone a keratorefractive procedure and: 1. Steepening by topography 2. Thinning of cornea 3. Shift in the position of thinnest portion of cornea 4. Change in refraction with increasing myopia 5. Development of myopic astigmatism 6. Development of irregular astigmatism 7. Loss of Best Spectacle Corrected Visual Acuity * At least two of the above criteria must be present. Inclusion Criteria Intacts: * Should the patient have undergone prior Intacs or other intra-corneal ring segment surgery for keratoconus or post-surgical ectasia at least 6 months prior, and is also experiencing at least two of the above ectasia symptoms, they can be included in the study. 1. These patients would have the choice of ring explant before Cross-Linking. 2. Cross-Linking may still be performed if the patient wishes to retain the rings. * Should a patient's situation due to factors such as significantly high myopia or astigmatism should warrant simultaneous placement of Intacs and cross-linking in the investigators opinion, then this option can be offered to the patient. Such interventions would be tracked as a different arm of the study. Inclusion Criteria RK/AK Fluctuation: * History of having undergone radial keratotomy (RK) and or astigmatic keratotomy (AK) surgery. * Expressing complaints about difficulties due to vision changing during the same day. * A difference in their Manifest Refraction (MRx) of greater than 0.75 D measured on the same day, at least 6 hours apart. * Intacs surgery will not be considered in patients with RK/AK.
Exclusion criteria
* Eyes classified as either normal, atypical normal, * Corneal pachymetry ≤ 350 microns at the thinnest point measured by Orbscan, Pentacam, or ultrasound in the eye to be treated * A history of chemical injury or delayed epithelial healing in the eye to be treated. * A known sensitivity to study medications * Patients with significant nystagmus or any other condition that would prevent a steady gaze during the treatment * Inability to cooperate with diagnostic tests. * Patients with a current condition that, in the investigator's opinion, would interfere with or prolong epithelial healing. * Taking Vitamin C (ascorbic acid) supplements within 1 week of the cross-linking treatment. * Patients who are unable to remain comfortable and stable, and tolerate a lid speculum for the appointed period of time for the procedure.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Visual Acuity | 2 years | Uncorrected visual acuity |
Countries
United States
Contacts
Primary ContactTravis A Johnson, Bachelor's
Backup ContactNancy A Tanchel, MD
Outcome results
None listed