Proof-of-concept Study for a New Intraocular Lens, MODEL C0001

Johnson & Johnson (J&J)

Status

Completed

Conditions

Cataract

Treatments

Device: Model C0001

Device: Model ZCB00

Study type

Interventional

Funder types

Industry

Identifiers

NCT05036070

PCOL-103-ARPV

Details and patient eligibility

About

This study is a 12-month, prospective, 2-arm (1 test & 1 control), randomized (1 test:1 control), bilateral, subject/evaluator-masked clinical investigation of the EPV IOL versus the standard TECNIS monofocal control IOL.

The study will be conducted at a minimum of one to a maximum of five sites in France, with a total of 40 evaluable subjects for the investigational lens group and 40 evaluable subjects for the control lens group participating in the sub-study. The peripheral and functional testing will be conducted on a sub-group of subjects who achieve binocular uncorrected distance visual acuity (UCDVA) of 0.2 logMAR or better and/or are able to perform the driving simulator-sickness testing as determined by patient response to the SSQ (Appendix D) at the first 1-month visit.

The eye implanted first will be considered the primary study eye (first eye). Subjects will be randomized to either the investigational IOL Model C0001 or the control IOL Model ZCB00 in both eyes.

Enrollment

113 patients

Sex

All

Ages

60 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age of study population between 60-75 years;
Bilateral cataracts for which cataract extraction and posterior chamber IOL implantation have been planned for both eyes;
Cataractous lens changes, as demonstrated by best-corrected distance visual acuity (BCDVA) of 0.50 decimal or worse (6/12 or 20/40 Snellen) either with or without a glare source present (e.g., Brightness Acuity Tester) or with significant cataract-related visual symptoms in the opinion of the investigator;
Potential postoperative best-corrected distance visual acuity (BCDVA) of 0.66 decimal (6/9 or 20/30 Snellen) or better;
Drives a car at least 1-2 times per month;
Corneal astigmatism:
- Normal corneal topography
- Predicted postoperative residual refractive cylinder based on a toric IOL calculator, taking surgically induced astigmatism (SIA) into account and using the posterior corneal astigmatism (PCA) option, must be less than 1.00 D in both eyes.
Clear intraocular media other than cataract in each eye;
Availability, willingness, sufficient cognitive awareness to comply with examination procedures;
Signed informed consent and HIPAA authorization or equivalent documentation necessary to comply with applicable privacy laws pertaining to medical treatment in the governing countries;
Ability to understand, read and write in French.

Exclusion criteria

Requiring an intraocular lens power needed to achieve emmetropia (spherical equivalent ± 0.50 D) outside the available range of +18.0 D to +30.0 D for the Model C0001 IOL or +16.0 D to +28.0 D for the Model ZCB00 IOL;
Pupil abnormalities (non-reactive, fixed pupils, or abnormally-shaped pupils);
Irregular corneal astigmatism;
Recent ocular trauma or ocular surgery that is not resolved/stable or may affect visual outcomes or increase risk to the subject;
Prior corneal refractive (LASIK, LASEK, RK, PRK, etc.) or intraocular surgery;
Subjects who may be expected to require retinal laser treatment during the study;
Corneal abnormalities such as stromal, epithelial or endothelial dystrophies that are predicted to cause visual acuity losses to a level of worse than 0.66 decimal (6/9 or 20/30 Snellen) during the study;
Inability to achieve keratometric corneal stability preoperatively as a result of recent contact lens usage;
Subjects with diagnosed degenerative visual disorders (e.g., retinal disorders such as macular degeneration) that are predicted to cause visual acuity losses to a level worse than 0.66 decimal (6/9 or 20/30 Snellen) during the study;
Subjects with conditions associated with increased risk of zonular rupture, including capsular or zonular abnormalities that may lead to IOL decentration or tilt, such as pseudoexfoliation, trauma, or posterior capsule defects;
Use of systemic or ocular medications that may affect vision;
Prior, current, or anticipated use during the course of the study of tamsulosin or silodosin (e.g., Flomax, Flomaxtra, Rapaflo) that may, in the opinion of the investigator, confound the outcomes or increase the risk to the subject (e.g., poor dilation or a lack of adequate iris structure to perform standard cataract surgery);
Inability to focus or fixate for prolonged periods of time (e.g., due to strabismus, nystagmus, etc.);
Poorly-controlled diabetes;
Acute, chronic, or uncontrolled systemic or ocular disease or illness that, in the opinion of the investigator, would increase the operative risk or confound the outcomes of the study (e.g., immunocompromised, connective tissue disease, suspected glaucoma, glaucomatous changes in the fundus or visual field, ocular inflammation, etc.); NOTE: Controlled ocular hypertension without glaucomatous changes (optic nerve cupping and visual field loss) is acceptable.
Neurological or neurodegenerative disorders that affect locomotion and cognitive function (e.g., Muscular disorders, Parkinson's disease, Alzheimer's disease etc.);
Use of mobility aids;
Motion Sickness Susceptibility Questionnaire Short-form (MSSQ-Short) score of ≥ 25;
Subject has condition(s) associated with the fluctuation of hormones that could lead to refractive changes;
Concurrent participation in any other clinical trial or participation within 30 days prior to the preoperative visit.