Clinical Study to Investigate Outcomes of Trifocal Toric IOL POD FT in Asian Eyes

Beaver-Visitec

Status

Active, not recruiting

Conditions

Cataract

Presbyopia

Lens Opacities

Treatments

Device: IOL implantation experimental

Study type

Interventional

Funder types

Industry

Identifiers

NCT03844828

PHY1901

Details and patient eligibility

About

Prospective, controlled, single-surgeon, single-center clinical study to compare visual acuity outcomes to data obtained in a similar study by the same principal investigator on the trifocal IOL POD F (study no. PHY1802, ClinicalTrials.gov ID: NCT03688425)

Full description

This is a prospective, controlled, single-surgeon, single-center clinical study, whereby patients undergoing routine cataract surgery will have mono- or bilateral implantation of trifocal toric intraocular lenses POD FT. The study is aimed to compare visual acuity outcomes the FineVision POD FT IOL to data obtained in a similar study by the same principal investigator on the trifocal FineVision POD F IOL (study no. PHY1802, ClinicalTrials.gov ID: NCT03688425), whereby patients undergoing routine cataract surgery will have bilateral implantation of trifocal intraocular lenses. The patients will either be implanted with the FineVision POD FT IOL in both eyes or, in case the corneal astigmatism in one of the two eyes of the same patient is too small to implant a toric lens, the FineVision POD F IOL will be implanted in this eye (both lenses: PhysIOL, Liège, Belgium).

The devices under investigation (FineVision POD FT and POD F) are trifocal glistening-free acrylic intraocular lenses (IOLs) manufactured by the sponsor of this study PhysIOL sa/nv. The main difference between the lenses is that that the POD FT IOL is the toric version of the POD F IOL. The IOLs will be implanted as part of the routine cataract surgery on patients suffering from cataract development.

Subjects participating in the trial will attend a total of 11 study visits (1 preoperative, 2 operative and 8 postoperative) over a period of 24 months. Subjects would have the option for unscheduled visits if required medically.

Primary endpoint data will be collected at the 6 months follow up visit and secondary endpoint data will be collected at the 1 Day, 1 Week, 1 month, 6, 12 and 24 months postoperative visits. Data analyses will be done after the last patient finished the final examination to support the study publication plan

Enrollment

100 estimated patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male or female adults ages 45 years or older on the day of screening who have cataract(s) in one or both eyes or suffer from presbyopia;
Regular corneal astigmatism ≥0.75 dioptres (measured by an automatic keratometer or biometer) in one or both eyes;
Capability to understand and sign an IRB approved informed consent form and privacy authorization;
Clear intraocular media other than cataract;
Calculated IOL power is within the range of the study IOLs;
Dilated pupil size large enough to visualize IOL axis markings postoperatively;
Willing and able to conform to the study requirements.

Exclusion criteria

Regular corneal astigmatism <0.75 dioptres (measured by an automatic keratometer or biometer) in both eyes
Irregular astigmatism;
Subjects with diagnosed degenerative visual disorders (e.g. macular degeneration or other retinal or optic disorders) that are predicted to cause future acuity losses to a level of 20/30 or worse;
Subjects with AMD suspicious eyes as determined by OCT examination;
Subjects who may be expected to require retinal laser treatment during the course of the study or at a greater risk of developing cystoid macular edema;
Previous intraocular or corneal surgery;
Traumatic cataract;
History or presence of macular edema;
Pregnant, lactating or, if able to bear children, unwilling to use medically acceptable birth control over the course of the study;
Concurrent or previous (within 30 days) participation in another drug or device investigation;
Instability of keratometry or biometry measurements;
Ocular hypertension or glaucoma;
Significant dry eye;
Unsuitable for study participation for any other reason, as determined by Investigator's clinical judgment (reason to be documented on eCRF).