Refractive Corneal Cross-linking for Progressive Keratoconus
Primary Purpose
Keratoconus
Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Customised CXL
Sponsored by
About this trial
This is an interventional treatment trial for Keratoconus focused on measuring progressive, cross-linking, customised, refractive
Eligibility Criteria
Inclusion Criteria:
- Patients with progressive stage I - III keratoconus
- Corrected distance visual acuity (CDVA) < 0.00 logMAR
Exclusion Criteria:
- Patients under the age of 18 years
- Active ocular surface disease
- Minimum corneal thickness < 375 µm
- Vulnerable groups
- Pregnancy
Sites / Locations
- Moorfields Eye Hospital NHS Foundation Trust
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Refractive CXL
Arm Description
Tomography-customised CXL
Outcomes
Primary Outcome Measures
Change in corrected distance visual acuity
LogMAR corrected vision in spectacles
Secondary Outcome Measures
Change in uncorrected distance visual acuity
LogMAR uncorrected vision without spectacles
Manifest refraction
Spectacle prescription
Tomography
Corneal Pentacam indices
Rates of keratitis
Complications of CXL
Full Information
NCT ID
NCT03531047
First Posted
May 8, 2018
Last Updated
August 31, 2020
Sponsor
Moorfields Eye Hospital NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT03531047
Brief Title
Refractive Corneal Cross-linking for Progressive Keratoconus
Official Title
A Prospective, Controlled Study of Refractive Corneal Cross-linking for Progressive Keratoconus
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2018 (Actual)
Primary Completion Date
November 2021 (Anticipated)
Study Completion Date
November 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Moorfields Eye Hospital NHS Foundation Trust
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Young patients with keratoconus face two problems: disease progression and corneal shape irregularity. Both underlie the 20% rate of corneal transplantation in keratoconics required to maintain useful vision.
Corneal collagen cross-linking (CXL) is a now the gold-standard treatment to halt disease progression. The aim is to strengthen the cornea to prevent further shape deterioration. For patients whose quality of vision has already suffered, standard CXL can generally only prevent further deterioration, rather than improving vision. Refractive CXL, a new iteration of CXL in which a bespoke treatment pattern is applied to the cornea, aims to smooth out surface irregularities thereby improving vision.
This primary objective of this study is to compare the visual outcome in patients with progressive keratoconus treated with refractive CXL, as compared with historical controls treated with standard CXL.
Detailed Description
Irregular astigmatism (irregular corneal shape leading to irregular focus) is a common cause of failure to achieve an adequate spectacle correction for many patients with corneal disease. For patients affected, rigid gas permeable contact lenses are the only means of visual rehabilitation. Not all patients tolerate rigid contact lens wear, and those that do are often uncomfortable and have a restricted wearing time.
Keratoconus, in which the corneal shape becomes progressively steeper and more irregular in the 2nd to 4th decades of life, is a common cause of irregular astigmatism. Disease progression in keratoconus can be stabilised with corneal collagen cross-linking (CXL), effective in 90% of cases. Pre-existing irregular astigmatism often remains after CXL, with many patients requiring rigid gas permeable contact lenses to regain good vision.
The investigators have recently demonstrated improvements in vision following simultaneous combined cross-linking with laser refractive surgery (TransPRK/CXL). The excimer laser is used to create a smoother, more regular focusing shape on the cornea to improve the quality of vision achieved in spectacles. Although effective, the downsides of using this approach are both the cost and limited availability of excimer laser equipment in the National Health Service (NHS) in the United Kingdom. Also, excimer laser smoothing works by removing corneal tissue. It is not yet known whether this tissue removal will have any detrimental effect on corneal shape stability post CXL.
As a cheaper and potentially more widely accessible alternative, refractive CXL aims to regularise the corneal surface by applying a bespoke treatment pattern based on pre-operative corneal surface shape (topography) scans. At least two-thirds of patients undergoing standard CXL already have impaired vision at the time treatment. The investigators are aiming to offer these patients both long-term stability of their keratoconus and an improvement in vision in a single treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Keratoconus
Keywords
progressive, cross-linking, customised, refractive
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
52 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Refractive CXL
Arm Type
Experimental
Arm Description
Tomography-customised CXL
Intervention Type
Procedure
Intervention Name(s)
Customised CXL
Other Intervention Name(s)
Riboflavin drops (drug): Vibex Rapid (Avedro Inc.)
Intervention Description
As for standard CXL, following mechanical removal of the corneal surface layer (epithelium), 0.1% riboflavin drops will be applied every 2 minutes for 10 minutes prior to ultraviolet A (UVA) irradiation - UVA power, distribution and timing as determined by analysis of Pentacam tomography scans. A bandage contact lens will be applied to encourage regrowth of the corneal surface and reduce post-operative pain.
Primary Outcome Measure Information:
Title
Change in corrected distance visual acuity
Description
LogMAR corrected vision in spectacles
Time Frame
24 months
Secondary Outcome Measure Information:
Title
Change in uncorrected distance visual acuity
Description
LogMAR uncorrected vision without spectacles
Time Frame
24 months
Title
Manifest refraction
Description
Spectacle prescription
Time Frame
24 months
Title
Tomography
Description
Corneal Pentacam indices
Time Frame
24 months
Title
Rates of keratitis
Description
Complications of CXL
Time Frame
24 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with progressive stage I - III keratoconus
Corrected distance visual acuity (CDVA) < 0.00 logMAR
Exclusion Criteria:
Patients under the age of 18 years
Active ocular surface disease
Minimum corneal thickness < 375 µm
Vulnerable groups
Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Daniel M Gore
Organizational Affiliation
Moorfields Eye Hospital NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Moorfields Eye Hospital NHS Foundation Trust
City
London
ZIP/Postal Code
EC1V 2PD
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
23258309
Citation
Gore DM, Shortt AJ, Allan BD. New clinical pathways for keratoconus. Eye (Lond). 2013 Mar;27(3):329-39. doi: 10.1038/eye.2012.257. Epub 2012 Dec 21.
Results Reference
result
PubMed Identifier
21349938
Citation
O'Brart DP, Chan E, Samaras K, Patel P, Shah SP. A randomised, prospective study to investigate the efficacy of riboflavin/ultraviolet A (370 nm) corneal collagen cross-linkage to halt the progression of keratoconus. Br J Ophthalmol. 2011 Nov;95(11):1519-24. doi: 10.1136/bjo.2010.196493. Epub 2011 Feb 24.
Results Reference
result
Learn more about this trial
Refractive Corneal Cross-linking for Progressive Keratoconus
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