CT Lucia 601 IOL Implantation in the Sulcus

Universitaire Ziekenhuizen KU Leuven62 enrolled

Overview

To perform a retrospective investigation of the CT Lucia 601 IOL implantation in the sulcus

The purpose of the study is to collect data that are parameters of post-IOL implantation safety: * Questionnaire on subjective quality of vision * Centration and anteroposterior position of the IOL (using biometry) * Presence and quantification of any inflammation or pigment present in the anterior chamber (flare meter) * Refractive outcome, with calculation of customized A-constant of the CT Lucia 601 IOL in-the-sulcus and quantification of higher-order aberrations (HOA) * General safety-parameters: * Visual acuity * Intra-ocular pressure * Presence of macular edema or retinal nerve fiber layer (RNFL) thinning (SD-OCT) * Any adverse ophthalmic events

Study Type

OBSERVATIONAL

Enrollment

Conditions

Cataract; Complicata Posterior Capsule Tear Lens Dislocation

Eligibility

Sex: ALLMin age: 18 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with an implantation of a CT Lucia 601 lens for different reasons: * During vitrectomy to treat a complicated cataract surgery and had the implantation of a CT Lucia 601 IOL in the sulcus or patients * During phaco surgery with a posterior capsule tear that necessitated the implantation of the implant lens in the sulcus * Explantation of an in-the-bag lens and implantation of a CT Lucia 601 as replacement lens (e.g. to treat opacification of the implant lens or intolerance of the implant lens). * Age : \> 18 years * Signed informed consent * Preoperative myopia less than 10 diopters * Implantation of the CT Lucia IOL at least six months earlier Exclusion Criteria: * History of uveitis * Ocular pathology or history that could influence the biometry of the effective lens position, such as ocular trauma with zonulolysis, congenital iris- or lens defects etc. * Any eye condition influencing the lens position (to be specified) according to the investigator

Locations (1)

UZ Leuven

Leuven, Vlaams Brabant, Belgium

Outcomes

Primary Outcomes

safety of the CT Lucia 601 IOL in the sulcus

determine whether the CT Lucia 601 IOL can be used safely in the sulcus

Time frame: 2019-2020

Data from ClinicalTrials.gov

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