Visual Acuity
Conditions
Brief summary
This will be a single center pilot study to evaluate appearance of the Meibomian glands.
Interventions
None listed
Sponsors
Johnson & Johnson Vision Care, Inc.
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes
Inclusion criteria
* Potential subjects must satisfy all of the following criteria to be enrolled in the study: 1. Healthy adult males and females, 18-40 years of age (inclusive) 2. The subject must read, understand, and sign the STATEMENT OF INFORMED CONSENT and receive a fully executed copy of the form 3. The subject must appear able and willing to adhere to the instructions set forth in this clinical protocol 4. The subject must agree not to participate in other clinical research for the duration of this study 5. The subject's optimal spherical equivalent distance refraction must be between +1.00 and -2.00 D in each eye 6. The subject's refractive cylinder must be ≤-1.00 DC in each eye 7. The subject must score less than 4 points (inclusive) in SPEED questionnaire
Exclusion criteria
* Potential subjects who meet any of the following criteria will be excluded from participating in the study: 1. Currently pregnant or lactating 2. Any systemic disease (e.g. Sjögren's Syndrome), allergies, infectious disease (e.g. hepatitis, tuberculosis), contagious immunosuppressive diseases (e.g. HIV), autoimmune disease (e.g. rheumatoid arthritis), or other diseases, by self-report, which are known to interfere with contact lens wear and/or participation in the study 3. Have had cataract surgery 4. Use of systemic medications (e.g. chronic steroid use) and any current use of ocular medications (e.g. lubricants, artificial tears) that would interfere with participation in the trial, at the Investigator's discretion 5. They have history (more than one week in total) of contact lens wear. 6. Any previous, or planned (during the course of the study) ocular surgery (e.g. radial keratotomy, PRK, LASIK, etc.) 7. Any ocular allergies, infections or other ocular abnormalities that are known to interfere with participation in the study. This may include, but not be limited to entropion, ectropion, extrusions, chalazia, recurrent styes, glaucoma, history of recurrent corneal erosions, aphakia, corneal distortion or keratoconus 8. History of allergy to sodium fluorescein or lissamine green 9. Any Grade 1.5 or greater slit lamp findings (e.g. oedema, corneal neovascularization, corneal staining, tarsal abnormalities, conjunctival injection) on the Efron Grading Scales or other ocular abnormality including Meibomian gland dysfunction (MGD) or blepharitis (Grade 1.0 or greater) 10. Meibomian gland atrophy exceeds 25% (inclusive) in either lower or upper eyelid 11. The central glands atrophy exceeds 25% (inclusive) 12. The number of Meibomian glands yielding liquid secretion (MGYLS) is 6 or less (applicable to Phase II subjects only) 13. Use of eye makeup on the days of the study visits 14. Participation in any pharmaceutical or medical device related clinical trial within 14 days prior to study enrolment 15. Employee or immediate family member of an employee of clinical site (e.g. Investigator, Coordinator, Technician)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Meibomian Gland Appearance - Area | up to 4-week follow-up | Meibomian gland appearance will be evaluated on both eyes using a custom image analysis algorithm, which calculates the area corresponding to individual and aggregated Meibomian glands. |
| Meibomian Gland Appearance - Mean Reflectivity | up to 4-week follow-up | Meibomian gland appearance will be evaluated on both eyes using a custom image analysis algorithm, which calculates the mean reflectivity of individual and aggregated Meibomian glands |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Lipid Layer Thickness (LLT) | up to 4-week follow-up | LLT will be measured using the LipiView® II instrument on the right eye only. |
| Non-Invasive Tear Break-Up Time (NIBUT) | up to 4-week follow-up | NIBUT will be evaluated using the Medmont E300 instrument, with three measurements taken for the right eye only, at least 30 seconds apart and the median recorded. |
| Tear Film Evaporation Rate | up to 4-week follow-up | Tear film evaporation rate will be assessed using the Eye-VapoMeter for 3 consecutive open eye measurements followed by 3 consecutive closed eye measurements. The mean for each method will be calculated. |
Countries
United Kingdom
Outcome results
None listed