CT Lucia 601 IOL Implantation in the Sulcus — CLUS  

Posterior Capsule Tear Clinical Trial

Official title: CT Lucia 601 IOL Implantation in the Sulcus

Status Terminated

Clinical Trial Summary

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

Clinical Trial Description

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 ;

Related Conditions & MeSH terms

• Cataract
• Cataract; Complicata
• Lens Dislocation
• Lens Subluxation
• Posterior Capsule Tear

• NCT number: NCT04796662
• Study type: Observational
• Source: Universitaire Ziekenhuizen KU Leuven
• Status: Terminated
• Start date: March 8, 2021
• Completion date: February 20, 2023