Presbyopia
Conditions
Keywords
Presbyopia, Accommodation, Near visual acuity, LASIK
Brief summary
The purpose of this study is to determine if the AcuFocus Corneal Inlay ACI 7000PDT will provide an effective method for the correction of presbyopia in patients who have normal distance vision but need a correction such as glasses or contact lenses to see clearly at near.
Detailed description
The loss of near vision and the ability to perform tasks that require near vision is part of the normal aging process. This natural transformation in the eye occurs as a result of the loss of accommodation of the crystalline lens, a condition known as presbyopia. The crystalline lens is responsible for the accommodative properties of the human eye, as established by Young in 1801, over 200 years ago.1 During accommodation, the ciliary muscle contracts, decreasing tension on the zonules, and allowing the crystalline lens to thicken, increasing its refractive power. This mechanism of accommodation and thickening of the lens provides the eye with adequate refractive power for near vision. The loss of accommodation with aging is the result of changes in the crystalline lens composition that prevent the natural accommodative process from occurring. This is associated with the gradual loss of near vision without external correction, generally in the form of spectacles. The AcuFocus™ ACI 7000PDT represents new technology based on the well-established concept of small-aperture optics. In early cameras, depth of focus was controlled by reducing the aperture through which light enters. The smaller the aperture, the greater the depth of focus will be. This concept also applies to the human eye. In the eye of a presbyopic emmetrope, the lens cannot accommodate sufficiently to focus the light rays from a near object onto a single point on the retina. Thus, a point object is imaged as a blur circle on the retina, and images of extended objects are degraded as well. If an opaque disc with a small aperture in the center is placed in front of the eye, the peripheral rays will be obscured while the central rays pass unaffected. Since peripheral rays enter the eye at a larger angle, they create a larger blur circle at the retinal image plane. Eliminating these peripheral rays reduces the size of the blur circle, improving image resolution. In presbyopic subjects, objects closer than arm's length are focused behind the retina, thus creating blurred retinal images (which are composed of blur circles). A small aperture inlay placed in front of the eye of these subjects allows them to see at near by reducing the size of the blur circle. AcuFocus, Inc. has developed a stationary intracorneal inlay designed to create a small aperture effect. The implant is intended to be placed intra-stromally either under a corneal flap or into a corneal pocket. Placement of the ACI will be centered over the pupil in the non-dominant eye. The ACI is expected to increase the depth of focus of the eye by reducing the circle of blur. Based on theoretical calculations of small aperture optics, the ACI is expected to provide presbyopic subjects with improvement of near and intermediate vision.
Interventions
DEVICEAcuFocus Corneal Inlay
Inlay implanted in cornea for improvement of near vision
Sponsors
AcuFocus, Inc.
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
45 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
1. Subjects must be natural emmetropes needing a minimum magnitude of +1.00D to +2.50D of reading add. 2. Subjects must have uncorrected near visual acuity worse than 20/40 and better than 20/100 in the eye to be implanted. 3. Subject must have distance visual acuity correctable to at least 20/20 in both eyes. 4. Subjects must have a preoperative spherical equivalent of plano defined as +0.50D to -0.75D with no more than 0.75D of refractive cylinder as determined by cycloplegic refraction in the eye to be implanted.
Exclusion criteria
1. Subjects with a difference of \> 1.00D between the spherical equivalent manifest refraction and the spherical equivalent cycloplegic refraction. 2. Subjects with anterior segment pathology, including cataracts, in the eye to be implanted. 3. Subjects with residual, recurrent, active ocular or uncontrolled eyelid disease, or any corneal abnormalities (including endothelial dystrophy, guttata, recurrent corneal erosion, etc.) in the eye to be implanted. 4. Subjects with ophthalmoscopic signs of keratoconus (or keratoconus suspect) in the eye to be implanted. 5. Subjects with a history of chronic dry eye not responding to therapy. 6. Subjects with distorted or unclear corneal mires on topography maps of the eye to be implanted. 7. Subjects who require canthotomy to generate a corneal flap in the eye to be implanted. 8. Subjects with macular degeneration, retinal detachment, or any other fundus pathology that would prevent an acceptable visual outcome in the eye to be implanted. 9. Subjects who have undergone previous intraocular or corneal surgery including cataract and LASIK surgery. 10. Subjects with a history of herpes zoster or herpes simplex keratitis. 11. Subjects who have a history of steroid-responsive rise in intraocular pressure, preoperative IOP \> 21 mmHg, glaucoma, or is a glaucoma suspect. 12. Subjects with a history of diagnosed diabetes, autoimmune disease, connective tissue disease, or clinically significant atopic syndrome. 13. Subjects on chronic systemic corticosteroids or other immunosuppressive therapy that may affect wound healing, and any immunocompromised subjects. 14. Subjects who are using ophthalmic medication(s) other than artificial tears for treatment of any ocular pathology including ocular allergy. 15. Subjects using systemic medications with significant ocular side effects. 16. Subjects who are pregnant, lactating, or of child-bearing potential and not practicing a medically approved method of birth control. 17. Subjects with known sensitivity to planned study concomitant medications. 18. Subjects who are participating in any other ophthalmic drug or device clinical trial during the time of this clinical investigation.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in Uncorrected Near Visual Acuity | 12 months | Percent of subjects who achieved UCNVA of 20/40 or better. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Improvement of Near Uncorrected Visual Acuity | 12 months | Mean subjective rating via questionnaire on 1 to 7 rating scale (1= very dissatisfied and 7 = very satisfied). |
Countries
Australia, Austria, Germany, New Zealand, Singapore, United Kingdom
Participant flow
Pre-assignment details
119 participants were consented for the study (enrolled), and 118 subsequently were implanted with the device (started) for the study.
Participants by arm
| Arm | Count |
|---|---|
| AcuFocus Corneal Inlay Implantation of the AcuFocus Corneal Inlay in emmetropic presbyopic patients.
AcuFocus Corneal Inlay ACI 7000PDT: Inlay implanted in cornea for improvement of near vision | 118 |
| Total | 118 |
Baseline characteristics
| Characteristic | AcuFocus Corneal Inlay |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 0 Participants |
| Age, Categorical Between 18 and 65 years | 118 Participants |
| Region of Enrollment Australia | 42 Participants |
| Region of Enrollment Austria | 24 Participants |
| Region of Enrollment Germany | 3 Participants |
| Region of Enrollment New Zealand | 18 Participants |
| Region of Enrollment Philippines | 11 Participants |
| Region of Enrollment Singapore | 9 Participants |
| Region of Enrollment United Kingdom | 11 Participants |
| Sex: Female, Male Female | 51 Participants |
| Sex: Female, Male Male | 67 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | — / — |
| other Total, other adverse events | 52 / 118 |
| serious Total, serious adverse events | 4 / 118 |
Outcome results
Primary
Improvement in Uncorrected Near Visual Acuity
Percent of subjects who achieved UCNVA of 20/40 or better.
Time frame: 12 months
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| AcuFocus Corneal Inlay | Improvement in Uncorrected Near Visual Acuity | 78.2 percentage of participants |
Secondary
Improvement of Near Uncorrected Visual Acuity
Mean subjective rating via questionnaire on 1 to 7 rating scale (1= very dissatisfied and 7 = very satisfied).
Time frame: 12 months
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| AcuFocus Corneal Inlay | Improvement of Near Uncorrected Visual Acuity | 4.7 units on a scale | Standard Deviation 1.7 |