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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 ;


Study Design


Related Conditions & MeSH terms


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

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