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Cataract
+2

Premium Trifocal IOL Comparative Analysis

Sponsored by Beaver-Visitec International, Inc.

About this trial

Last updated 4 years ago

Study ID

PHY1705

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
45+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 4 years ago

What is this trial about?

Short and long-term analysis of the refraction correction and optical image quality of modern premium intraocular lenses (IOLs) with the establishment of a database for quality assurance and optimization the computation constants of the lens power.

What are the participation requirements?

Yes

Inclusion Criteria

- Availability, willingness and sufficient cognitive awareness to comply with examination procedures

- Bilateral implantation of one of the following IOL models

- Alcon PanOptix (TFNT00)

- PhysIOL FineVision (POD F)

- PhysIOL FineVision (POD F GF)

- Uneventful cataract surgery with first clinical outcomes in the expected range

- Patient included in Premium IOL study protocol by signed informed consent

No

Exclusion Criteria

- Age of patient <45 years

- Irregular astigmatism

- Postoperative manifested astigmatism of >1.0 D

- Difficulty for cooperation (distance from their home, general health condition)

- Clinically significant glaucoma

- Clinically significant macular degeneration, clinically significant macular edema or proliferative diabetic retinopathy

- Patients with keratoconus or keratectasia

- Any ocular comorbidity having a significant effect on the postoperative clinical outcomes

- History of ocular trauma or prior ocular surgery including refractive procedures

- Capsule or zonular abnormalities that may affect postoperative centration or tilt of the lens (e.g. pseudoexfoliation syndrome, chronic Uveitis, Marfan's syndrome)

- Pupil abnormalitis (non-reactive, tonic pupils, abnormally shaped pupils or pupils that do not dilate under mesopic/scotopic conditions)

- AMD

- Intraoperative complications like capsular rupture etc.

- Patients who do not give informed consent

Locations

Location

Status