Three different protocols for inducing corneal crosslinks in subjets with progressive keratoconus will be evaluated in this randomised clinical study.
Riboflavin does not penetrate the intact corneal epithelium. Corneal cross linking (CXL) is typically performed using the so-called "Dresden protocol". The Dresden protocol states 30 minutes of UVA-radiation (3mW/cm2) but a 10 minute irradiation protocol (9mW/cm2) is frequently used. Both of the protocols involve mechanical removal of the epithelium over the central 8 mm of the corneal surface. The first days after treatment therefore involves some degree of pain, often intense, and the presence of a healing epithelial defect may be associated with development of infiltrates in the cornea. A number of approaches have been evaluated in order to promote riboflavin penetration through the intact epithelium, of which iontophoresis appears most promising. Keratoconic corneas are thin at the cone location and sometimes it is difficult to maintain the safety margin of 400 microns during corneal crosslinking. Instead of using isotonic standard riboflavin, a swelling effect of the cornea can be obtained by using hypotonic riboflavin. However, the latter has been indicated as less effective in the process of inducing cross links. Eighty-one of 81 patients of various degrees of keratoconus will be randomised to one of the following groups: 1) CXL (UVA 9mW/cm2) using isotonic riboflavin, or 2) CXL (UVA 9mW/cm2) using hypotonic riboflavin or 3) Iontophoresis with Ricrolin with following CXL (UVA 9mW/cm2). Hypothesis: i) CXL with hypotonic riboflavin or CXL with Ricrolin administered by iontophoresis or CXL with isotonic riboflavin is non-inferior compared to standard CXL with isotonic riboflavin. ii) The morphological structure post-CXL in the three different groups will be similar without any significant differences. The iontophoresis-assisted treatment arm has been interrupted due to low efficacy in halting disease progression. The results have been published.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
54
CXL treatment with UVA-radiation (9mW/cm2) with a 10 minute irradiation protocol.
CXL protocol with isotonic riboflavin
CXL protocol with hypotonic riboflavin
Skåne University Hospital
Lund, Skåne County, Sweden
Postoperative change in visual acuity
Uncorrected visual acuity (UCVA) and best spectacle corrected visual acuity (BSCVA)
Time frame: Patients will be evaluated 1, 6, 12 and 24 months after treatment.
Postoperative change in Kmax
Maximum corneal steepness
Time frame: Patients will be evaluated 1, 6, 12 and 24 months after treatment.
Postoperative change in astigmatism
Corneal astigmatism
Time frame: Patients will be evaluated 1, 6, 12 and 24 months after treatment.
postoperative change in corneal nerve cell density
Corneal nerve cell density will be evaluated using confocal microscopy
Time frame: Confocal microscopy will be performed at 6 and 12 months.
Postoperative change in Keratocyte cell density
Keratocyte cell density will be evaluated using confocal microscopy
Time frame: Confocal microscopy will be performed at 6 and 12 months.
Postoperative change in endothelial cell count
Endothelial cell count will be evaluated using confocal microscopy
Time frame: Confocal microscopy will be performed at 6 and 12 months.
Postoperative change in demarcation lines
Identification of the demarcation lines with confocal microscopy will help establishing how deep was the effect of the CXL treatment.
Time frame: Confocal microscopy will be performed at 6 and 12 months.
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CXL protocol with iontophoresis and ricrolin
Postoperative change in the corneal thickness during CXL treatment
Corneal pachymetry is the process of measuring the thickness of the cornea
Time frame: Corneal pachymetry will be evaluated before and then every 5 minutes during 30 minutes under CXL treatment.