Investigation of the Presbia Flexivue Microlens™

Presbyopia Clinical Trial

Official title:

Prospective, Non-randomized, Unmasked, Multicenter Clinical Investigation of the Presbia Flexivue Microlens™ for the Improvement of Near Vision in Emmetropic Presbyopes

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02110472
• Other study ID #: CLP-12-001
• Status: Active, not recruiting
• Phase: Phase 3
• First received: April 8, 2014
• Last updated: September 26, 2016
• Start date: May 2014
• Est. completion date: February 2019

Study information

• Verified date: September 2016
• Source: PresbiBio, LLC
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

The Presbia Flexivue Microlens is a corneal inlay.

Description:

Presbyopia is a multifactorial physiological aging mechanism that leads to a progressive functional loss of near vision. In addition to the use of reading glasses for presbyopia, a wide variety of procedures have been investigated by ophthalmologists to correct this refractive error. Cornea laser surgery with multifocal patterns or monovision approaches were developed including LASIK, PresbyLASIK, photorefractive keratectomy (PRK), laser epithelial keratomileusis (LASEK), thin-flap femto-LASIK or sub-Bowman's keratomileusis (SBK). Conductive keratoplasty (CK), clear lens extraction or cataract surgery using multifocal, pseudo-accommodative intraocular lenses (IOLs) or monovision monofocal IOLs are also some of the techniques that have been used for the treatment of presbyopia.

Corneal laser surgery and CK are minimally invasive methods, but they provoke irreversible changes of the corneal anatomy, whereas scleral surgery and clear lens extraction are more invasive techniques. The necessity to develop a minimally invasive, reversible, and safe surgical technique with an easy learning curve for patients between 45 and 60 years, led to the development of refractive intracorneal lenses (inlays) (such as the AcuFocus, Inc. KAMRA™, ReVision Optics® PresbyLens®, and the Presbia Flexivue Microlens™) placed inside the corneal stroma. These inlays are refractive lenses that have a central zone free of refractive power and a peripheral zone with a standard positive refractive power. These inlays are inserted inside the corneal stroma of the non-dominant eye, generally offering two different focal points, one for the far vision and a different for the near vision respectively. The pocket of the cornea is created using a laser (details to be provided later in this protocol).

The Presbia Flexivue Microlens is intended to improve near vision and decrease dependence on reading glasses in presbyopic adults who are tolerant of monovision (as evaluated by participation in a monovision tolerance trial (5 to 7 days minimum)), who require a reading add of +1.50 D to +3.50 D, who have MRSE between +1.00 D and 0.75 D with no more than 0.75 D of refractive cylinder, and who have stable MRSE within 0.50 D over the past 12 months.

Objective: The primary objective of this study is to evaluate the safety and effectiveness of the Presbia Flexivue Microlens™ (hereinafter referred to as the "Microlens") implanted in presbyopes for improvement of near vision.

Investigational Plan: This is a prospective, non-randomized, unmasked, multicenter clinical investigation. A total of 412 subjects at up to 11 investigational sites in the United States will undergo insertion of the Microlens in non-dominant eyes, and will be followed through 36 months postoperative (assuming an estimated 10% per year lost to follow-up). Each site will contribute a targeted minimum of 20 treated subjects, but no more than 25% of the total subjects treated in the study. Data on a minimum of 300 subjects with 24 month data will be submitted as part of the Premarket Approval; all subjects will be followed through 36 months postoperative. Subjects from outside the United States will not be enrolled in this study.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 412
• Est. completion date: February 2019
• Est. primary completion date: December 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 45 Years to 60 Years

Eligibility

Inclusion Criteria:

• Subjects must be emmetropes with presbyopia, between = 45 years and = 60 years of age at time of eligibility visit.

• Subjects must need a reading add of +1.50 D to +3.50 D.

• Subjects must have uncorrected near visual acuity of 20/50 or worse.

• Subjects must have near visual acuity correctable to 20/20 or better in each eye.

• Subjects must have distance visual acuity correctable to 20/25 or better in each eye.

• Subjects must have a preoperative spherical equivalent of +1.00 D to -0.75 D with no more than 0.75 D of refractive cylinder as determined by cycloplegic refraction in each eye.

• Subjects must have a photopic pupil size of > 1.6 mm in the eye to be implanted.

Exclusion Criteria:

• Subjects in whom the non-dominant eye cannot be determined using one of the methods identified in the test of ocular dominance.

• Subjects who do not complete the monovision tolerance trial (minimum of 5 to 7 days).

• Subjects who report that they were not completely satisfied with their vision during the monovision tolerance trial.

• Subjects who report that they experienced debilitating or significant visual symptoms such as halos, glare, double vision, etc. during the monovision tolerance trial.

• Subjects with a difference of = 1.00 D between the spherical equivalent manifest refraction and the spherical equivalent cycloplegic refraction.

• Subject with a preferred near working distance of < 35 cm or > 45 cm.

• Subjects with corneal thickness < 500 microns in the eye to be implanted.

• Subjects with clinically significant anterior segment pathology, including cataracts, in either eye.

• Subjects with residual, recurrent, active ocular or uncontrolled eyelid disease or any progressive corneal abnormalities (including endothelial dystrophy, guttata in the central cornea, etc.) in the eye to be treated.

• Subjects with keratoconus (or keratoconus suspect), amblyopia, recurrent erosion syndrome or corneal dystrophy in the eye to be treated.

• Subjects with a history of chronic dry eye not controlled on therapy or with superficial punctuate keratitis (SPK) grade > II (i.e., greater than mild) based on Oxford Grading Scale in the eye to be treated.

• Subjects with abnormal corneal mires on topography maps of the eye to be treated.

• Subjects who require canthotomy to generate a corneal tunnel in the eye to be treated.

• Subjects with progressive retinal pathology with a reasonable chance of causing a reduction in BCVA from preoperative in the eye to be treated.

• Subjects who have undergone previous intraocular or corneal surgery including cataract and refractive surgery (e.g., LASIK surgery) in either eye.

• Subjects using ophthalmic medication(s) other than artificial tears for treatment of ocular pathology.

• Subjects with a history of autoimmune disease, connective tissue disease, or clinically significant atopic syndrome.

• Subjects with a history of herpes zoster or herpes simplex keratitis.

• Subjects with a history of steroid-responsive rise in intraocular pressure (IOP), or a preoperative IOP > 21 mmHg or glaucoma.

• Subjects with distorted, non-reactive, or decentered pupils.

• Subjects taking medication for the control of diabetes.

• Subjects on chronic systemic or topical corticosteroids or other immunosuppressive therapy that may affect wound healing, and any immuno-compromised subjects (use of intranasal steroids for seasonal allergies are acceptable).

• Subjects using systemic medications (e.g., amiodarone) or medications with significant ocular side effects.

• Subjects who are pregnant, or are considering becoming pregnant during the time of the study.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Presbyopia

Intervention

Device:
• Corneal inlay
Presbia Flexivue Microlens implantation in corneal pocket created in nondominant eyes of emmetropic presbyopes.

Locations

Country	Name	City	State
United States	Assil Eye Institute	Beverly Hills	California
United States	Cleveland Eye Clinic	Brecksville	Ohio
United States	Kraft Eye Institute	Chicago	Illinois
United States	Hoopes Vision, Laser Correction Center	Draper	Utah
United States	The Eye Center	Fairfax	Virginia
United States	Physicians Protocol	Greensboro	North Carolina
United States	Berkeley Eye and Laser Center	Houston	Texas
United States	Gordon-Weiss-Schanzlin	La Jolla	California
United States	Maloney Vision Institute	Los Angeles	California
United States	Stanford Eye and Laser Center	Palo Alto	California
United States	Center for Sight	Sarasota	Florida

Sponsors (1)

Lead Sponsor	Collaborator
PresbiBio, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Uncorrected near visual acuity - operated eyes	Uncorrected near visual acuity at 40 cm of 20/40 or better	24 months postoperative	No
Secondary	Uncorrected near visual acuity - operated eyes	- Number of lines of improvement uncorrected near visual acuity	24 months postoperative	No

External Links

•   Website dedicated to patient recruitment (approved by WIRB on 4/3/2014).