C-CROSS: Efficacy of Customized Corneal Cross-linking vs. Standard Corneal Cross-linking
Study Details
Study Description
Brief Summary
The standard or Dresden protocol was established in 2003 and treats the entire cornea. However, recent ultra-structural research showed that keratoconus is localized. Therefore, treating only the affected zone and minimalizing the risk of damaging surrounding tissues would be beneficial.
The objective of this study is to evaluate whether the effectiveness of customized cross-linking (cCXL) is non-inferior to standard accelerated cross-linking (sCXL) in terms of flattening of the cornea and halting keratoconus progression.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
In 2003 Wollensak et al used corneal cross-linking (CXL) in humans to halt the progression of keratoconus. During the procedure the top layer of the cornea, the epithelium, is debrided. Then the cornea is soaked with riboflavin, a photosensitizer. Hereafter a 9.0 mm diameter Ultraviolet-A (UVA) beam radiates the cornea for 30 minutes with a fluence of 3 mW/cm2 resulting in a total energy of 5,4 J/cm2. This protocol is called the Dresden protocol. Currently, accelerated versions of the Dresden protocol are used in common practice. There are different accelerated protocols with fluences of 9mW/cm2, 10mW/cm2 and 15 mW/cm2. The higher the fluence, the shorter the treatment time, however according to the Bunsen-Roscoe reciprocity law the total amount of energy stays the same.During the procedure oxygen radicals are formed that interact with the surrounding molecules, leading to the formation of new chemical bounds between the collagen fibrils (i.e. corneal crosslinks). The final goal of the procedure is to cause the cornea to stiffen and achieve flattening of the treated region.
For any treatment, it is imperative that the unaffected region of the tissue is not unnecessarily treated by an intervention or drug application. To minimalize the risk of damage to surrounding tissues it would be beneficial that the UVA beam is restricted to the affected, keratoconic zone in the patient's cornea. This can be achieved by customizing the beam shape and size in a way that only the degenerated zone is treated, i.e. by customized cross-linking (cCXL). Recently published studies provide clinical evidence that similar clinical outcomes (amount of corneal flattening) can be achieved when only the cone is treated instead of the entire cornea.They also show the potential benefits of cCXL, e.g. the treatment is patient-specific, a smaller surface of the cornea is irradiated, lower incidence of corneal haze, a faster reepithelialisation and a shorter procedure time. However, none of these studies are randomized and study results are limited by using small sample sizes. Therefore, we feel that there is a great need for a randomized controlled trial with an appropriate design and sample size to confirm these findings.
The aim of this study is to investigate if cCXL is non-inferior to sCXL (10 mW/cm2) in terms of flattening of the corneal surface and halting the disease progression.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Customized crosslinking In the customized corneal cross-linking protocol (cCXL) a patient-specific treatment pattern, based on the patient's Pentacam images, will be used to treat the cornea. The CXL pattern exists out of 3 concentric circles and is centered on the cone. To estimate the cone location a combination of the thinnest corneal point, maximum anterior elevation and maximum posterior elevation is used. The epithelium is debrided with alcohol within the marked zone. After the application of riboflavin each circle receives a different amount of energy, which gradually decreases with increasing circle size. The procedure is done with the Avedro Mosaic CXL device (Avedro, Inc. Waltham, Massachusetts, United States). |
Procedure: Customized crosslinking
In the customized corneal cross-linking protocol (cCXL) a patient-specific treatment pattern, based on the patient's Pentacam images, will be used to treat the cornea. The CXL pattern exists out of 3 concentric circles and is centered on the cone. To estimate the cone location a combination of the thinnest corneal point, maximum anterior elevation and maximum posterior elevation is used. The epithelium is debrided with alcohol within the marked zone. After the application of riboflavin each circle receives a different amount of energy, which gradually decreases with increasing circle size.
The procedure is done with the Avedro Mosaic CXL device (Avedro, Inc. Waltham, Massachusetts, United States).
|
| Active Comparator: Standard crosslinking In the standard corneal cross-linking protocol (sCXL) the epithelium is debrided with alcohol over a region with a diameter of 9.0 mm. After the application of riboflavin the cornea is irradiated with UVA with a fluence of 10 mW/cm2 during 9 minutes with a diameter of 9.0 mm, resulting in a total energy of 5.4 J/cm2. The procedure is done with the Avedro Mosaic CXL device (Avedro, Inc. Waltham, Massachusetts, United States). |
Procedure: Standard crosslinking
In the standard corneal cross-linking protocol (sCXL) the epithelium is debrided with alcohol over a region with a diameter of 9.0 mm. After the application of riboflavin the cornea is irradiated with UVA with a fluence of 10 mW/cm2 during 9 minutes with a diameter of 9.0 mm, resulting in a total energy of 5.4 J/cm2.
The procedure is done with the Avedro Mosaic CXL device (Avedro, Inc. Waltham, Massachusetts, United States).
|
Outcome Measures
Primary Outcome Measures
- Change in maximum keratometry (Kmax) [12 months postoperatively]
Kmax is measured with Scheimpflug photography (Pentacam® HR, OCULUS Optikgeraete GmbH, Wetzlar, Germany)
Secondary Outcome Measures
- Visual acuity [at baseline, 4 weeks, 3 months, 6 months and 12 months postoperatively]
Measured with ETDRS
- Refraction [at baseline and 12 months postoperatively]
Change in spherical equivalent
- Depth and size of demarcation line [at 4 weeks and 12 months postoperatively]
Measured with AS OCT
- Pachymetry [at baseline, 4 weeks, 3 months, 6 months and 12 months postoperatively]
Measured with the Pentacam HR
- Zonal Kmax [at baseline, 4 weeks, 3 months, 6 months and 12 months postoperatively]
The analysis of a 3.0 mm zone centered on Kmax measured with the Pentacam HR
- DUCK score [at baseline, 4 weeks, 3 months, 6 months and 12 months postoperatively]
Dutch Crosslinking for Keratconus Score is based on changes in 5 clinical parameters that are routinely assessed: age, visual acuity, refraction error, keratometry, and subjective patient experience. Each items is scored from 0 to 2 and cutoffs are determined by clinical experience.
- ABCD grading system [at baseline, 4 weeks, 3 months, 6 months and 12 months postoperatively]
Anterior radius of curvature (A), Posterior radius of curvature (B), Corneal pachymetry at thinnest point (C), Distance best corrected vision (D), and a modifier (-) for no scarring, (+) for scarring that does not obscure iris details and (++) for scarring that obscures iris details
- Success/failure rate [at 12 months postoperatively]
Failure is defined as progression of the disease after CXL. Progression is defined as an increase in Kmax >1D over 12 months, an increase in K1 and/or K2 >1D over 12 months and thinning and/or an increase in the rate of corneal thickness change from the periphery to the thinnest point >10% over 12 months
- Mean endothelial cell loss [at 6 and 12 months postoperatively]
Measured using specular microscopy photography
- Rate of reepithelialisation [4 days postoperatively]
evaluated with fluorescein and blue light, a slit lamp image is taking to perform quantitative morphometric surface analysis
- Patient Reported Outcomes Measures (PROMs) [at baseline, 3 months, 6 months and 12 months postoperatively]
Health-related quality of life as measured by HUI3 (Health Utility Index Mark 3) questionnaire
- Patient Reported Outcomes Measures (PROM) [at baseline, 3 months, 6 months and 12 months postoperatively]
Patient satisfaction and vision-specific quality of life as measured by National Eye Institute Visual Function Questionnaire (NEI VFQ-25)
- Patient Reported Outcomes Measures (PROM) [at baseline, 3 months, 6 months and 12 months postoperatively]
Patient satisfaction and vision-specific quality of life as measured by Keratoconus Outcome Research Questionnaire (KORQ)
- Pain after crosslinking [4 days postoperatively]
measured with the short form of the McGill Pain Questionnaire (SF-MPQ)
- Quality Adjusted Life Years (QALYs) [baseline until 12 months postoperatively]
Calculated based on generic health-related quality of life, using the EQ-5D-5L questionnaire
- Quality Adjusted Life Years (QALYs) [baseline until 12 months postoperatively]
Calculated based on generic health-related quality of life, using the HUI-3 questionnaire
- Costs per patient [baseline until 12 months postoperatively]
Cost per patient, including valuation of resource use by using the Dutch guidelines for cost-analyses or cost prices provided by the medical center.
- Incremental cost-effectiveness ratios (ICERs): QALY [baseline until 12 months postoperatively]
Evaluation of cost-effectiveness by using calculated costs per quality-adjusted life years (QALYs)
- Incremental cost-effectiveness ratios (ICERs): NEI VFQ-25 [baseline until 12 months postoperatively]
Calculated costs per clinically improved patient on the NEI VFQ-25 questionnaire
- Incremental cost-effectiveness ratios (ICERs): Kmax [baseline until 12 months postoperatively]
incremental healthcare costs per patient with a reduction in Kmax of ≥ 1D after crosslinking
- Incremental cost-effectiveness ratios (ICERs): visual acuity [baseline until 12 months postoperatively]
incremental healthcare costs per patient with clinical improvement in (un-) corrected distance visual acuity
- Budget impact [baseline until 12 months postoperatively]
Reported as a difference in costs. Different scenario's will be compared to investigate the impact of various levels of implementation (e.g. 25%, 50%, 75% of eligible patients)
Eligibility Criteria
Criteria
Inclusion Criteria:
- Progressive keratoconus based on an increase of maximum keratometry (Kmax) of 1 diopter (D) over a time period of 12 months
Exclusion Criteria:
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Corneal scarring
-
Corneal disease other than keratoconus
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History of corneal surgery (e.g. refractive surgery, corneal transplantation, intracorneal ring segments)
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Patient unwilling or unable to give informed consent, unwilling to accept randomization or inability to complete follow-up (e.g. hospital visits) or comply with study procedures
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Insufficient corneal thickness including epithelium < 375 µm
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Pregnancy
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Among patients in whom both eyes are eligible only the first eye which is undergoing corneal cross-linking is enrolled in the study
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Participation in another clinical study
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Maastricht University Medical Center (MUMC+) | Maastricht | Limburg | Netherlands | 6229 HX |
| 2 | University Medical Center Groningen | Groningen | Netherlands | 9713 GZ | |
| 3 | University Medical Center Utrecht | Utrecht | Netherlands | 3584 CX |
Sponsors and Collaborators
- Maastricht University Medical Center
- ZonMw: The Netherlands Organisation for Health Research and Development
Investigators
- Principal Investigator: R.M.M.A. Nuijts, MD, PhD, Department of Ophthalmology, Maastricht University Medical Center (MUMC+)
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- NL73003.068.20