Healthy Controls, Keratoconus
Conditions
Brief summary
The purpose of this study is to investigate changes in the corneal thickness of scleral contact lens wearers in a keratoconic (KC) population and compare to age-matched controls. The hypothesis is that scleral contact lens wear is associated with low levels of corneal hypoxia including measurable changes in corneal thickness. Corneal thickness will be altered post scleral lens wear compared to pre-lens wear and the amount of alteration will correlate to the fitting characteristics in the central zone of the scleral lenses. We propose to take a sample of keratoconic and control participants, fit them in scleral lenses, and to measure topographic corneal thickness after 8-10 hours of scleral lens wear after three weeks of wear, to compare two instruments in the measurement of corneal thickness, and to compare the effects of varying central corneal clearance of the scleral lens on corneal thickness.
Detailed description
The purpose of this study is to investigate changes in the corneal thickness of scleral contact lens wearers in a keratoconic (KC) population and compare to age-matched controls. The hypothesis is that scleral contact lens wear is associated with low levels of corneal hypoxia including measurable changes in corneal thickness. This will be a prospective, dispensing study design. The study will involve up to 20 keratoconic participants and up to 20 age matched controls. Participants will attend 1 screening/fitting visit wearing their habitual contact lenses where the two test lens designs (350 and 450microns) will be fitted. There will then be a delivery visit for each design (randomly selected) and a single follow up visit after 8-10 hours of scleral lens wear, three weeks later. A washout period of a minimum of 48 hours will be applied between the cross-over of each lens design. Lenses to be worn in this study will be made of Boston XO material and are approved by Health Canada. The lenses will have a diameter of 14.8-17.0mm with a high and low sagittal depth in the corneal zone. As to which of the two lenses is being assessed, both the investigator and the participant will be masked as the assistant will provide the lenses in an unlabeled case. Masking the investigator will prevent bias when measuring corneal thickness and analyzing the data. The objectives of this study are to take a sample of keratoconic and control participants, fit them in scleral lenses, and to measure topographic corneal thickness after 8-10 hours of scleral lens wear after three weeks of wear, to compare two instruments in the measurement of corneal thickness, and to compare the effects of varying central corneal clearance of the scleral lens on corneal thickness. Secondary objectives include comparing ocular physiological outcomes between the two test lens designs. Corneal thickness will be altered post scleral lens wear compared to pre-lens wear and the amount of alteration will correlate to the fitting characteristics in the central zone of the scleral lenses.
Interventions
DEVICEZenLens™
The ZenLens™ semi-scleral lenses are manufactured by Alden Optic Laboratories Inc., Lancaster, NY. They will be made in Boston XO material.
DEVICEZen™ RC
The Zen™ RC semi-scleral lenses are manufactured by Alden Optic Laboratories Inc., Lancaster, NY. They will be made in Boston XO material.
Sponsors
Bausch & Lomb Incorporated
University of Waterloo
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
(Test Group): * Had been diagnosed with keratoconus in at least one eye. * Is at least 18 years of age and has full legal capacity to volunteer. * Has read and understood the information consent letter. * Is willing and able to follow instructions and maintain the appointment schedule. Inclusion Criteria (Control Group) * Had been NOT diagnosed with keratoconus in at least one eye. * Is at least 18 years of age and has full legal capacity to volunteer. * Has read and understood the information consent letter. * Is willing and able to follow instructions and maintain the appointment schedule.
Exclusion criteria
(Test Group): * Is using any topical medications that will affect ocular health. * Has any ocular pathology or severe insufficiency of lacrimal secretion (severe dry eyes) that would affect the wearing of contact lenses. * Has persistent, clinically significant corneal or conjunctival staining using sodium fluorescein dye. * Has any clinically significant lid or conjunctival abnormalities and active neovascularization. * Is aphakic. * Has undergone penetrating keratoplasty. * Is participating in any other type of eye related clinical or research study. * Has any known allergies or sensitivity to the diagnostic pharmaceuticals or products, such as fluorescein, used in this study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Corneal Thickness | 6 weeks | Corneal thickness after 8-10 hours of scleral contact lens wear will be measured with the Spectralis OCT and Oculus Pentacam |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Visual acuity | 6 weeks | Both high and low contrast visual acuity will be measured before and after 8-10 hours of scleral contact lens wear |
| Conjunctival redness | 6 weeks | Conjunctival redness will be measured with the Keratograph before and after 8-10 hours of scleral lens wear |
| Corneal and conjunctival staining | 6 weeks | Corneal and conjunctival staining will be assessed with the Keratograph and biomicroscope before and after 8-10 hours of scleral lens wear |
| Tear biochemistry: proteases and cytokines | 6 weeks | The level of proteases (MMP-1, MMP-9) and cytokines (IL-1, IL-6, IL-8, TNFα) in each of the tear samples collected from the lenses will be measured using the Meso Scale Discovery System (MSD-ECL) before and after 8-10 hours of scleral lens wear. |
| Tear biochemistry: cell count | 6 weeks | Polymorphonuclear leukocyte (PMN) cells in each of the tear samples collected from the lenses will be analyzed and counted using the BD FACS Calibur™ Flow Cytometer and Bright-Line Hemacytometer before and after 8-10 hours of scleral lens wear. |
Countries
Canada
Contacts
Primary ContactKirsten S Carter, BSc OD
Outcome results
None listed