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Rotational Stability Analysis of a Toric Monofocal IOL

Sponsored by Beaver-Visitec International, Inc.

About this trial

Last updated 4 years ago

Study ID

PHY2013

Status

Completed

Type

Interventional

Phase

N/A

Placebo

No

Accepting

18-75 Years
50+ Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 6 years ago

What is this trial about?

This is a single-center, prospective PMCF study whereby patients undergoing routine cataract surgery will have monolateral implantation of hydrophilic monofocal toric intraocular lens Ankoris.

What are the participation requirements?

Yes

Inclusion Criteria

- Cataracteous Eyes with no comorbidity

- Regular corneal astigmatism >1 dioptre and <3D determined by an automatic keratometer (regularity determined by the topography of the keratometry).

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

- Signed informed consent •>50 years old

No

Exclusion Criteria

- Acute or chronic disease or illness that would increase risk or confound study results (e.g. diabetes mellitus (with retinopathy), immunocompromised, glaucoma etc…)

- Any ocular comorbidity

- 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, Marfan's syndrome)

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

Locations

Location

Status